Cas 309935-03-3,2-trifluoroacetamidoethyl 2,2',3,6,6'-penta-O-benzyl-3',4'-O-isopropylidene-β-D-lactoside

309935-03-3

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Basic information

Product Name: 2-trifluoroacetamidoethyl 2,2',3,6,6'-penta-O-benzyl-3',4'-O-isopropylidene-β-D-lactoside
Synonyms: 2-trifluoroacetamidoethyl 2,2',3,6,6'-penta-O-benzyl-3',4'-O-isopropylidene-β-D-lactoside
CAS NO:309935-03-3
Molecular Formula:
Molecular Weight: 972.065
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: 2-trifluoroacetamidoethyl 2,2',3,6,6'-penta-O-benzyl-3',4'-O-isopropylidene-β-D-lactoside(CAS DataBase Reference)
NIST Chemistry Reference: 2-trifluoroacetamidoethyl 2,2',3,6,6'-penta-O-benzyl-3',4'-O-isopropylidene-β-D-lactoside(309935-03-3)
EPA Substance Registry System: 2-trifluoroacetamidoethyl 2,2',3,6,6'-penta-O-benzyl-3',4'-O-isopropylidene-β-D-lactoside(309935-03-3)

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: 309935-03-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 309935-03-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,9,9,3 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 309935-03:
(8*3)+(7*0)+(6*9)+(5*9)+(4*3)+(3*5)+(2*0)+(1*3)=153
153 % 10 = 3
So 309935-03-3 is a valid CAS Registry Number.

309935-03-3Upstream product

383-63-1 ethyl trifluoroacetate,

309935-03-3Downstream Products

309935-03-3Relevant academic research and scientific papers

A novel approach to functionalization of allyl aglycon. Effective synthesis of selectively protected 2-aminoethyl lactoside, a common building block for the synthesis of carbohydrate chains of glycolipids

Kononov,Cheshev,Nifant'ev

, p. 1305 - 1309 (2000)

A novel approach to the funclionalizaiion of aglycon in allyl glycosides is described. The method comprises ozonolysis of the double bond in the allyl group, leading to the corresponding aldehyde, and subsequent transformation of the latter into the corre

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