Cas 432547-05-2,4-Cyclohexene-1,2,3-triol, 6-amino-4-methyl-, (1R,2R,3R,6S)-rel- (9CI)

432547-05-2

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Basic information

Product Name: 4-Cyclohexene-1,2,3-triol, 6-amino-4-methyl-, (1R,2R,3R,6S)-rel- (9CI)
Synonyms: 4-Cyclohexene-1,2,3-triol, 6-amino-4-methyl-, (1R,2R,3R,6S)-rel- (9CI)
CAS NO:432547-05-2
Molecular Formula: C7H13NO3
Molecular Weight: 159.18302
EINECS: N/A
Product Categories: ALCOHOL
Mol File: 432547-05-2.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4-Cyclohexene-1,2,3-triol, 6-amino-4-methyl-, (1R,2R,3R,6S)-rel- (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: 4-Cyclohexene-1,2,3-triol, 6-amino-4-methyl-, (1R,2R,3R,6S)-rel- (9CI)(432547-05-2)
EPA Substance Registry System: 4-Cyclohexene-1,2,3-triol, 6-amino-4-methyl-, (1R,2R,3R,6S)-rel- (9CI)(432547-05-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 432547-05-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 432547-05-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,2,5,4 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 432547-05:
(8*4)+(7*3)+(6*2)+(5*5)+(4*4)+(3*7)+(2*0)+(1*5)=132
132 % 10 = 2
So 432547-05-2 is a valid CAS Registry Number.

432547-05-2Upstream product

432547-05-2Downstream Products

432547-05-2Relevant academic research and scientific papers

Synthesis of an α-fucosidase inhibitor, 5a-carba-β-L-fucopyranosylamine, and fucose-type α- and β-DL-valienamine unsaturated derivatives

Ogawa, Seiichiro,Watanabe, Maiko,Maruyama, Ayako,Hisamatsu, Seiichi

, p. 749 - 752 (2002)

Discovery of a very potent α-fucosidase inhibitor 5a-carba-α-L-fucopyranosylamine (1) led to preparation of its β-anomer 4 and the respective unsaturated derivatives, fucose-type α- and β-valienamines (5 and 6), in order to elucidate the structure-activit

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