| Identification | Back Directory | [Name]
(2R,4R)-N-Boc-4-hydroxypyrrolidine-2-carboxylic acid | [CAS]
135042-12-5 | [Synonyms]
BOC-D-CISHYP-OH
Boc-cis-D-Hyp-OH
cis-Boc-D-Hyp-OH
N-Boc-D-cis-Hyp-OH
N-Boc-cis-D-Hyp-OH
ATTERCOP-CHM AT700573
Boc-cis-4-hydroxy-D-proL
BOC-CIS-4-HYDROXY-D-PROLINE
N-BOC-CIS-4-HYDROXY-D-PROLINE
N-BOC-CIS-6-HYDROXY-D-PROLINE
cis-N-Boc-4-hydroxy-D-proline
N-T-BOC-CIS-4-HYDROXY-D-PROLINE
(2R,4R)-N-BOC-4-HYDROXY-D-PROLINE
N-Boc-cis-4-hydroxy-D-proline 95+%
(Tert-Butoxy)Carbonyl cis-D-Hyp-OH
(2R,4R)-N-Boc-cis-4-hydroxy-D-proline
(2R,4R)N-Boc-trans-4-hydroxy-D-proline
N-α-(t-Butoxycarbonyl)-cis-4-hydroxy-D-proline
N-ALPHA-BUTOXYCARBONYL-CIS-4-HYDROXY-D-PROLINE
cis-N-(tert-Butoxycarbonyl)-4-hydroxy-D-proline
(4R)-1-(tert-Butoxycarbonyl)-4-hydroxy-D-proline
(2r,4r)-n-boc-4-hydroxypyrrolidine-2-carboxylic acid
(2R,4R)-N-Boc-4-hydroxy-2-pyrrolidinecarboxylic acid
BOC-(2R,4R)-(+)-4-HYDROXYPYRROLIDINE-2-CARBOXYLIC ACID
(2R,4R)-N-Boc-4-hydroxypyrrolidine-2-carboxylic acid USP/EP/BP
(2R,4R)-1-tert-Butoxycarbonyl-4-hydroxypyrrolidine-2-carboxylic acid
(2R,4R)-4-Hydroxypyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester
(2R,4R)-N-ALPHA-T-BUTOXYCARBONYL-4-HYDROXYPYRROLIDINE-2-CARBOXYLIC ACID
1,2-Pyrrolidinedicarboxylic acid, 4-hydroxy-, 1-(1,1-diMethylethyl) ester, (2R,4R)-
1,2-Pyrrolidinedicarboxylic acid, 4-hydroxy-, 1-(1,1-diMethylethyl) ester, (2R-cis)- | [EINECS(EC#)]
621-971-2 | [Molecular Formula]
C10H17NO5 | [MDL Number]
MFCD02094407 | [MOL File]
135042-12-5.mol | [Molecular Weight]
231.25 |
| Chemical Properties | Back Directory | [Melting point ]
145°C | [alpha ]
+48～+52°(c=0.67,MeOH,24℃) | [Boiling point ]
390.9±42.0 °C(Predicted) | [density ]
1.312 | [storage temp. ]
2-8°C | [form ]
powder to crystal | [pka]
3.80±0.40(Predicted) | [color ]
White to Light yellow | [optical activity]
[α]22/D +50.0°, c = 1 in methanol | [InChIKey]
BENKAPCDIOILGV-RNFRBKRXSA-N |
| Hazard Information | Back Directory | [Chemical Properties]
White solid | [Uses]
N-Boc-cis-4-hydroxy-D-proline can be used:
- As a starting material in the synthesis of DNA mimicking pyrrolidine peptide nucleic acid (PNA) analog.
- In the synthesis of biologically important macrocyclic dilactones.
- As an intermediate in the synthesis of histamine H3?receptor antagonists.
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