Cas 404351-01-5,D-2-O-benzyl-3-O-cyclohexylcarbamoyl-4-(N,N'-dicyclohexylureido)-4-deoxy-1-O-methyl-5,6-O-trichloroethylidene-chiro-inositol

404351-01-5

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Basic information

Product Name: D-2-O-benzyl-3-O-cyclohexylcarbamoyl-4-(N,N'-dicyclohexylureido)-4-deoxy-1-O-methyl-5,6-O-trichloroethylidene-chiro-inositol
Synonyms:
CAS NO:404351-01-5
Molecular Formula:
Molecular Weight: 745.184
EINECS: N/A
Product Categories: N/A

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: D-2-O-benzyl-3-O-cyclohexylcarbamoyl-4-(N,N'-dicyclohexylureido)-4-deoxy-1-O-methyl-5,6-O-trichloroethylidene-chiro-inositol(CAS DataBase Reference)
NIST Chemistry Reference: D-2-O-benzyl-3-O-cyclohexylcarbamoyl-4-(N,N'-dicyclohexylureido)-4-deoxy-1-O-methyl-5,6-O-trichloroethylidene-chiro-inositol(404351-01-5)
EPA Substance Registry System: D-2-O-benzyl-3-O-cyclohexylcarbamoyl-4-(N,N'-dicyclohexylureido)-4-deoxy-1-O-methyl-5,6-O-trichloroethylidene-chiro-inositol(404351-01-5)

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: 404351-01-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 404351-01-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,4,3,5 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 404351-01:
(8*4)+(7*0)+(6*4)+(5*3)+(4*5)+(3*1)+(2*0)+(1*1)=95
95 % 10 = 5
So 404351-01-5 is a valid CAS Registry Number.

404351-01-5Upstream product

404351-01-5Downstream Products

404351-01-5Relevant academic research and scientific papers

Unexpected formation of a D-chiro inositol from a L-chiro precursor

Miethchen, Ralf,Sowa, Christian,Michalik, Manfred

, p. 8637 - 8639 (2001)

In a one-step procedure, L-1-O-benzyl-2-O-methyl-chiro-inositol (1) was acetalized to the L-muco-inositol derivatives 2, 3 and D-2-O-benzyl-3-O-cyclohexylcarbamoyl-4-(N,N′-dicyclohexylureido)-4- deoxy-1-O-methyl-5,6-O-trichloroethylidene-chiro-inositol (4

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