Cas 1309566-40-2,N-[2-N,N-dimethylamino-2-deoxy-3,4,6-tri-O-methyl-β-D-glucopyranosyl]-N'-(3,5-bis-trifluoromethyl)phenyl urea

1309566-40-2

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Basic information

Product Name: N-[2-N,N-dimethylamino-2-deoxy-3,4,6-tri-O-methyl-β-D-glucopyranosyl]-N'-(3,5-bis-trifluoromethyl)phenyl urea
Synonyms: N-[2-N,N-dimethylamino-2-deoxy-3,4,6-tri-O-methyl-β-D-glucopyranosyl]-N'-(3,5-bis-trifluoromethyl)phenyl urea
CAS NO:1309566-40-2
Molecular Formula:
Molecular Weight: 503.442
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: N-[2-N,N-dimethylamino-2-deoxy-3,4,6-tri-O-methyl-β-D-glucopyranosyl]-N'-(3,5-bis-trifluoromethyl)phenyl urea(CAS DataBase Reference)
NIST Chemistry Reference: N-[2-N,N-dimethylamino-2-deoxy-3,4,6-tri-O-methyl-β-D-glucopyranosyl]-N'-(3,5-bis-trifluoromethyl)phenyl urea(1309566-40-2)
EPA Substance Registry System: N-[2-N,N-dimethylamino-2-deoxy-3,4,6-tri-O-methyl-β-D-glucopyranosyl]-N'-(3,5-bis-trifluoromethyl)phenyl urea(1309566-40-2)

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: 1309566-40-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1309566-40-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,9,5,6 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1309566-40:
(9*1)+(8*3)+(7*0)+(6*9)+(5*5)+(4*6)+(3*6)+(2*4)+(1*0)=162
162 % 10 = 2
So 1309566-40-2 is a valid CAS Registry Number.

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1309566-40-2Relevant academic research and scientific papers

Novel carbohydrate-based bifunctional organocatalysts for nucleophilic addition to nitroolefins and imines

Puglisi, Alessandra,Benaglia, Maurizio,Raimondi, Laura,Lay, Luigi,Poletti, Laura

, p. 3295 - 3302 (2011)

Glucosamine has been selected as a cheap and readily available chiral scaffold for the synthesis of a series of novel enantiomerically pure bifunctional organocatalysts bearing a tertiary amino group in proximity to a (thio)urea group. The catalytic behav

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