| 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. |
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Spectrum Chemical Manufacturing Corp.
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Energy Chemical
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021-58432009 400-005-6266 |
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http://www.energy-chemical.com |
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Carbosynth
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www.carbosynth.com |
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A.J Chemicals
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www.ajchemicals.com |
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