Identification | Back Directory | [Name]
D-GLUCOHEPTONO-1,4-LACTONE | [CAS]
60046-25-5 | [Synonyms]
Einecs 262-037-0 GLUCOHEPTONOLACTONE GLUCOHEPTONO 1-4 LACTONE D-GLUCOHEPTONO-1,4-LACTONE a-D-Glucohepto-1,4-lactone ALPHA-GLUCOHEPTONIC LACTONE α-d-glucoheptonic γ-lactone ALPHA-D-GLUCOHEPTONIC LACTONE Glucoheptonic Acid γ-Lactone A-D-GLUCOHEPTONIC ACID G-LACTONE alpha-D-Glucoheptonic gamma-lactone (2ξ)-D-Glucoheptonic Acid γ-Lactone (2.xi)-D-gluco-heptono-gamma-lactone D-GLYCERO-D-GULOHEPTONO-GAMMA-LACTONE Alpha-D-Glucoheptonic acid Gamma-lactone alpha-D-Glucoheptonic acid gamma-lactone,99% D-gluco-Heptonic acid, .gamma.-lactone, (2.xi.)- D-glycero-D-gulo-heptono-1,4-lactone, D-gluco-heptono-gamma-lactone | [EINECS(EC#)]
262-037-0 | [Molecular Formula]
C7H12O7 | [MDL Number]
MFCD00005390 | [MOL File]
60046-25-5.mol | [Molecular Weight]
208.17 |
Hazard Information | Back Directory | [Chemical Properties]
white fine crystalline powder | [Uses]
It is used in the synthesis of Howiinol A and its analogs. Howiinol A was one of the active antitumor constituents from the root and stem bark of Goniothamus howii (Annonaceae), and it was synthesized in 9 steps from α-D-glucoheptonic γ-lactone. Twenty-six analogs were also synthesized in searching for new antitumor compounds with high potency. |
|
Company Name: |
Spectrum Chemical Manufacturing Corp.
|
Tel: |
021-021-021-67601398-809-809-809 15221380277 |
Website: |
www.spectrumchemical.com/oa_html/index.jsp?minisite=10020&respid=22372&language=us |
Company Name: |
Energy Chemical
|
Tel: |
021-58432009 400-005-6266 |
Website: |
http://www.energy-chemical.com |
Company Name: |
Carbosynth
|
Tel: |
+86 512 6260 5585 |
Website: |
www.carbosynth.com |
|