Cas 90406-10-3,2-deoxy-3,4-O-isopropylidene-2-(trifluoroacetamido)-D-glucose dibenzyl acetal

90406-10-3

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Basic information

Product Name: 2-deoxy-3,4-O-isopropylidene-2-(trifluoroacetamido)-D-glucose dibenzyl acetal
Synonyms: 2-deoxy-3,4-O-isopropylidene-2-(trifluoroacetamido)-D-glucose dibenzyl acetal
CAS NO:90406-10-3
Molecular Formula:
Molecular Weight: 513.511
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-deoxy-3,4-O-isopropylidene-2-(trifluoroacetamido)-D-glucose dibenzyl acetal(CAS DataBase Reference)
NIST Chemistry Reference: 2-deoxy-3,4-O-isopropylidene-2-(trifluoroacetamido)-D-glucose dibenzyl acetal(90406-10-3)
EPA Substance Registry System: 2-deoxy-3,4-O-isopropylidene-2-(trifluoroacetamido)-D-glucose dibenzyl acetal(90406-10-3)

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: 90406-10-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 90406-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,0 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 90406-10:
(7*9)+(6*0)+(5*4)+(4*0)+(3*6)+(2*1)+(1*0)=103
103 % 10 = 3
So 90406-10-3 is a valid CAS Registry Number.

90406-10-3Upstream product

90406-06-7 2-deoxy-3,4:5,6-di-O-isopropylidene-2-(trifluoroacetamido)-aldehydo-D-glucose dibenzyl acetal

90406-10-3Downstream Products

90406-13-6 5,6-di-O-acetyl-2-deoxy-3,4-O-isopropylidene-2-(trifluoroacetamido)-aldehydo-D-glucose dibenzyl acetate

90406-10-3Relevant academic research and scientific papers

ONE-FLASK SYNTHESIS OF TRIACETALATED ALDOHEXOSES WITH 2,2-DIALKOXYPROPANE AND P-TOLUENESULFONIC ACID

Kiso, Makoto,Kondo, Akihiro,Kondo, Yumi,Hasegawa, Akira

, p. 121 - 128 (2007/10/02)

2-Deoxy-D-arabino-hexose and some N-protected 2-amino-2-deoxy-D-glucose derivatives were each treated with 2,2-dimethoxy- or 2,2-dibenzyloxy-propane in 1,4-dioxane in the presence of p-toluenesulfonic acid at 60-70 deg.The major products were acyclic, dim

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