Cas 1254946-88-7,dimethyl (1S,2S,4S,5S)-4-(2,3-dimethylphenylamino)-5-hydroxycyclohexane-1,2-dicarboxylate

1254946-88-7

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Basic information

Product Name: dimethyl (1S,2S,4S,5S)-4-(2,3-dimethylphenylamino)-5-hydroxycyclohexane-1,2-dicarboxylate
Synonyms: dimethyl (1S,2S,4S,5S)-4-(2,3-dimethylphenylamino)-5-hydroxycyclohexane-1,2-dicarboxylate
CAS NO:1254946-88-7
Molecular Formula:
Molecular Weight: 335.4
EINECS: N/A
Product Categories: N/A
Mol File: 1254946-88-7.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: dimethyl (1S,2S,4S,5S)-4-(2,3-dimethylphenylamino)-5-hydroxycyclohexane-1,2-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: dimethyl (1S,2S,4S,5S)-4-(2,3-dimethylphenylamino)-5-hydroxycyclohexane-1,2-dicarboxylate(1254946-88-7)
EPA Substance Registry System: dimethyl (1S,2S,4S,5S)-4-(2,3-dimethylphenylamino)-5-hydroxycyclohexane-1,2-dicarboxylate(1254946-88-7)

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: 1254946-88-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1254946-88-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,4,9,4 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1254946-88:
(9*1)+(8*2)+(7*5)+(6*4)+(5*9)+(4*4)+(3*6)+(2*8)+(1*8)=187
187 % 10 = 7
So 1254946-88-7 is a valid CAS Registry Number.

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1254946-88-7Relevant articles and documents

Synthesis of non glycosidic nucleobase-sugar mimetics

Hatton, Wilfried,Arosio, Daniela,Re, Marco,Giudici, Daniele,Bernardi, Anna,Seneci, Pierfausto

, p. 1284 - 1300 (2010)

Biologically active organic molecules acting as nucleoside mimics are frequently encountered in pharmaceutical research. They are either synthetic heterocycles, which miss the sugar-derived interactions with the active site of the nucleoside-binding prote

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