Fmoc-Asn(Trt)-OH
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Fmoc-Asn(Trt)-OH Eigenschaften
- Schmelzpunkt:
- 201-204 °C(lit.)
- alpha
- -16 º (c=1, MeOH)
- Siedepunkt:
- 858.1±65.0 °C(Predicted)
- Dichte
- 1.271±0.06 g/cm3(Predicted)
- Brechungsindex
- -19 ° (C=1, DMF)
- storage temp.
- 2-8°C
- L?slichkeit
- <0.00005g/l
- pka
- 3.79±0.10(Predicted)
- Aggregatzustand
- powder to crystal
- Farbe
- White to Almost white
- Optische Aktivit?t
- [α]20/D 15.0±1°, c = 1% in methanol
- Wasserl?slichkeit
- <0.00005g/L
- BRN
- 4343823
- InChIKey
- KJYAFJQCGPUXJY-UUWRZZSWSA-N
- SMILES
- C(O)(=O)[C@H](CC(N)=O)N(C(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O)C(C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1
- CAS Datenbank
- 132388-59-1(CAS DataBase Reference)
Sicherheit
- Risiko- und Sicherheitserkl?rung
- Gefahreninformationscode (GHS)
R-S?tze: | 53 | ||
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S-S?tze: | 24/25-61 | ||
RIDADR | UN 3077 9 / PGIII | ||
WGK Germany | 2 | ||
F | 3-10 | ||
HS Code | 2924 29 70 | ||
HazardClass | IRRITANT | ||
Toxizit?t | LD50 orally in Rabbit: > 2000 mg/kg |
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Alarmwort | Warnung | ||||||||||||||
Gefahrenhinweise |
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Sicherheit |
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Fmoc-Asn(Trt)-OH Chemische Eigenschaften,Einsatz,Produktion Methoden
S-S?tze Betriebsanweisung:
S24/25:Berührung mit den Augen und der Haut vermeiden.Beschreibung
Fmoc-Asn(Trt)-OH prevents the possibility of the amide side chain from undergoing dehydration side reactions during activation, especially with carbodiimide reagents. Fmoc-Asn(Trt)-OH dissolves readily in all standard peptide synthesis reagents, while Fmoc-Asn-OH is only somewhat soluble in NMP or DMF. The trityl group is removed with TFA. This reaction is usually complete within 1 hour at room temperature, but is slower when the Asn(Trt) residue in at the N-terminal of the peptide. In these cases, the deprotection reaction should be extended to 2 hours.Chemische Eigenschaften
white crystal powdeVerwenden
Fmoc-Asn(Trt)-OH, is an amino acid derivative used in chemical synthesis and peptide chemistry.synthetische
Synthesis of Fmoc-Asn(Trt)-OH:Step 1: Crystallization to form N'-Trityl-L-asparagine crystals.
Step 2: Centrifugation to extract N'-Trityl-L-asparagine crystals.
Step 3: Washing to remove residual starting materials in the synthesis.
Step 4: Extraction to obtain N-Acetyl-L-asparagine.
Step 5: Centrifugation to extract N'-Trityl-L-asparagine.
Step 6: Drying to obtain the final product.
This synthesis method effectively removes residual synthetic materials such as trifluoroacetic acid, maleic anhydride, and epichlorohydrin, which are similar in chemical properties to N-Acetyl-L-asparagine, from the product during the production process. The purification method is simple and the product obtained has high purity.
Fmoc-Asn(Trt)-OH Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
Fmoc-Asn(Trt)-OH Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.
Global( 443)Lieferanten
Firmenname | Telefon | Land | Produktkatalog | Edge Rate | |
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Lanxi Xingnuo Import and Export Trading Co., Ltd | +86-15888978871 +86-13901546477 |
sales@xingnuotraders.com | China | 163 | 58 |
Chengdu ZY Biochemical Technology Co., Ltd. | +86-86-2888626688 +8618980008884 |
xuehaiying@zybiochem.com | China | 125 | 58 |
Wuhan senwayer century chemical Co.,Ltd | +undefined-27-86652399 +undefined13627115097 |
market02@senwayer.com | China | 909 | 58 |
Hangzhou ICH Biofarm Co., Ltd | +86-0571-28186870; +undefined8613073685410 |
sales@ichemie.com | China | 1010 | 58 |
Chengdu Baishixing Science and Technology Industry Co.,Ltd | +86-15008457246 +86-15008457246 |
yuki@cd-bsx.com | China | 53 | 58 |
Sichuan HongRi Pharma-Tech Co.,Ltd | +86-028-64841719 +8617390183901 |
daisy@enlaibio.com | China | 1106 | 58 |
Capot Chemical Co.,Ltd. | +86-(0)57185586718 +86-13336195806 |
sales@capot.com | China | 29793 | 60 |
Shanghai Daken Advanced Materials Co.,Ltd | +86-371-66670886 |
info@dakenam.com | China | 18940 | 58 |
Nanjing ChemLin Chemical Industry Co., Ltd. | 025-83697070 |
product@chemlin.com.cn | CHINA | 3009 | 60 |
ATK CHEMICAL COMPANY LIMITED | +undefined-21-51877795 |
ivan@atkchemical.com | China | 32965 | 60 |
132388-59-1()Verwandte Suche:
Trityl candesartan
Thiokohlensure, Anhydrosulfid mit Methylthiohypochlorit
Toluol-4-sulfonsure
4-tert-Butylhydrogen-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-aspartat
9-Fluorenylmethyl chloroformate
Trityl Irbesartan
Trityl candesartan cilexetil
Nalpha-Fmoc-Ndelta-trityl-L-glutamine
D(-)-Asparaginmonohydrat
L-Fmoc-Aspartic acid alpha-tert-butyl ester
2-Phenylpropen
N6-(tert-Butoxycarbonyl)-N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-lysin
Asparagin
Asparaginase
Chlortriphenylmethan
Carbonylsulfid
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-phenyl-L-alanin
N-(9-Fluorenylmethoxycarbonyloxy)succinimide
- N-ALPHA-FMOC-N-GAMMA-TRITYL-L-ASPARAGINE
- FMOC-ASPARAGINE(TRT)
- FMOC-ASN(XAN)-OH
- FMOC-L-ASN(TRITYL)
- FMOC-L-ASPARGINE(TRITYL)
- FMOC-L-ASPARAGINE(TRITYL)
- FMOC-L-ASPARAGINE (TRT)
- FMOC-N-GAMMA-XANTHYL-L-ASPARAGINE
- Nalpha-fluorenylmethoxycarbonyl-Ngamma-trityl-L-asparagine
- Nα-(9-Fluorenylmethoxycarbonyl)-Nγ-trityl-L-asparagine, Nα-Fmoc-Nγ-trityl-L-asparagine
- N-(9-Fluorenylmethyloxycarbonyl)-N-trityl-L-asparagine ,98%
- Fmoc-L-Asparagine(Trt)-OH
- Fmoc-N-trityl-L-asparagine ,98%
- Fmoc-N-trityl-L-aspa
- Fmoc-Asparagine(Trt)-OH
- L-ASPARAGINE-N-FMOC, N-BETA-TRITYL
- Nalpha-Fmoc-Ngamma-trityl-L-asparagine Fmoc-Asn(Trt)-OH
- N^a-FMoc-N^y-trityl-L-asparagine, 97%
- FMoc-N-trityl-L-aspaD23-Ragine
- (S)-2-((((9H-Fluoren-9-yl)Methoxy)carbonyl)aMino)-4-oxo-4-(tritylaMino)butanoic acid
- FMoc-Asn(Tre)
- Fmoc-Asn(Trt)-OH >=97.0% (sum of enantiomers, HPLC)
- Fmoc-Asn(Trt)-OH(CAS:132388-59-1)
- FMOC-NG-TRITYL-L-ASPARAGINE
- FMOC-N-GAMMA-TRITYL-L-ASPARAGINE
- FMOC-N-TRITYL-L-ASPARAGINE
- FMOC-N-BETA-TRITYL-L-ASPARAGINE
- Nα-(9-Fluorenylmethoxycarbonyl)-Nγ-trityl-L-asparagine
- Na-(9-Fluorenyl Methoxy Carbonyl)-Ng-Trityl-L-Asparagine
- na-fmoc-N-gamma-trityl-L-asparagine
- N-alpha-(9-fluorenylmethoxycarbonyl)-N-gamma-trit
- N-α-Fmoc-N-γ-trityl-L-asparagine
- N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-N-&
- FMOC-N-TRITYL-L-ASPARAGINE 97+%
- N-FMOC-N4-TRITYL-L-ASPARAGINE
- N-(9-Fluorenylmethoxycarbonyl)-N-trityl-L-aspara
- L-Asparagine N-|beta|-Trityl-15N2-N-alpha-FMOC
- L-Asparagin, N(2)-((9H-fluoren-9-ylmethoxy)carbonyl)- N-(triphenylmethyl)-
- N2-[(9H-FLUOREN-9-YLMETHOXY)CARBONYL]-N-(TRIPHENYLMETHYL)-L-ASPARAGINE
- N-.ALPHA.-FMOC-N-.GAMMA.-XANTHYL-L-ASPARAGINE
- N-α-Fmoc-β-trityl-L-asparagine
- L-Asparagine N-β-Trityl-15N2-N-α-FMOC
- Nα-[(9H-Fluoren-9-ylmethoxy)carbonyl]-Nγ-trityl-L-asparagine
- Nα-Fmoc-Nγ-trityl-L-asparagine≥ 99.7% (HPLC, Chiral purity)
- N-FMOC-L-ASN(TRT)-OH
- N-(9-FLUORENYL METHOXY CARBONYL)-N-TRITYL-L-ASPARAGINE
- N-ALPHA-[(9H-FLUOREN-9-YLMETHOXY)CARBONYL]-N-GAMMA-TRITYL-L-ASPARAGINE
- N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-BETA-TRITYL-L-ASPARAGINE
- N-ALPHA-9-FLUORENYLMETHOXYCARBONYL-N-OMEGA-TRITYL-L-ASPARAGINE
- NALPHA-(9-FLUORENYLMETHOXYCARBONYL)-NR-TRITYL-L-ASPARAGINE
- N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-N-GAMMA-TRITYL-L-ASPARAGINE
- N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-N-BETA-TRITYL-L-ASPARAGINE
- N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-N-BETA-XANTHYL-L-ASPARAGINE
- N ALPHA-T-BUTOXYCARBONYL-N GAMMA-TRITYL-L-ASPARAGINE
- N-ALPHA-FMOC-N-BETA-TRITYL-L-ASPARAGINE
- (2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-[(triphenylmethyl)carbamoyl]propanoic acid
- 4-[[9H-fluoren-9-ylmethoxy(oxo)methyl]amino]-4-oxo-2-[(triphenylmethyl)amino]butanoic acid
- Nα-[(9H-Fluoren-9-ylmethoxy)carbonyl]-Nγ-trityl-L-asparagine>