Cas 141418-28-2,1,6-anhydro-2-O-benzyl-3,4-dideoxy-D-threo-hexopyranoside and 1,6-anhydro-2-O-benzyl-3,4-dideoxy-D-erythro-hexopyranoside

141418-28-2

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Basic information

Product Name: 1,6-anhydro-2-O-benzyl-3,4-dideoxy-D-threo-hexopyranoside and 1,6-anhydro-2-O-benzyl-3,4-dideoxy-D-erythro-hexopyranoside
Synonyms:
CAS NO:141418-28-2
Molecular Formula:
Molecular Weight: 220.268
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: 1,6-anhydro-2-O-benzyl-3,4-dideoxy-D-threo-hexopyranoside and 1,6-anhydro-2-O-benzyl-3,4-dideoxy-D-erythro-hexopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: 1,6-anhydro-2-O-benzyl-3,4-dideoxy-D-threo-hexopyranoside and 1,6-anhydro-2-O-benzyl-3,4-dideoxy-D-erythro-hexopyranoside(141418-28-2)
EPA Substance Registry System: 1,6-anhydro-2-O-benzyl-3,4-dideoxy-D-threo-hexopyranoside and 1,6-anhydro-2-O-benzyl-3,4-dideoxy-D-erythro-hexopyranoside(141418-28-2)

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: 141418-28-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 141418-28-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,4,1 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 141418-28:
(8*1)+(7*4)+(6*1)+(5*4)+(4*1)+(3*8)+(2*2)+(1*8)=102
102 % 10 = 2
So 141418-28-2 is a valid CAS Registry Number.

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141418-28-2Downstream Products

141418-28-2Relevant academic research and scientific papers

Reactivity, Selectivity, and Synthesis of 4-C-Silylated Glycosyl Donors and 4-Deoxy Analogues

J?ger Pedersen, Martin,Pedersen, Christian Marcus

, p. 2689 - 2693 (2021)

A method for introducing dimethylphenylsilyl at the 4-position in carbohydrates has been developed. Two C-silylated glycosyl donors were prepared via levoglucosenone, starting from cellulose. The glycosylation properties were studied using three glucoside

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