Cas 121820-60-8,(2R,3R,4S,5R,6S)-3,4,5-Tris-benzyloxy-2-benzyloxymethyl-6-((E)-3,7-dimethyl-octa-2,6-dienyloxy)-tetrahydro-pyran

121820-60-8

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Basic information

Product Name: (2R,3R,4S,5R,6S)-3,4,5-Tris-benzyloxy-2-benzyloxymethyl-6-((E)-3,7-dimethyl-octa-2,6-dienyloxy)-tetrahydro-pyran
Synonyms:
CAS NO:121820-60-8
Molecular Formula:
Molecular Weight: 676.893
EINECS: N/A
Product Categories: N/A
Mol File: 121820-60-8.mol
Article Data: 1

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: (2R,3R,4S,5R,6S)-3,4,5-Tris-benzyloxy-2-benzyloxymethyl-6-((E)-3,7-dimethyl-octa-2,6-dienyloxy)-tetrahydro-pyran(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R,4S,5R,6S)-3,4,5-Tris-benzyloxy-2-benzyloxymethyl-6-((E)-3,7-dimethyl-octa-2,6-dienyloxy)-tetrahydro-pyran(121820-60-8)
EPA Substance Registry System: (2R,3R,4S,5R,6S)-3,4,5-Tris-benzyloxy-2-benzyloxymethyl-6-((E)-3,7-dimethyl-octa-2,6-dienyloxy)-tetrahydro-pyran(121820-60-8)

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: 121820-60-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 121820-60-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,8,2 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 121820-60:
(8*1)+(7*2)+(6*1)+(5*8)+(4*2)+(3*0)+(2*6)+(1*0)=88
88 % 10 = 8
So 121820-60-8 is a valid CAS Registry Number.

121820-60-8Upstream product

121820-60-8Downstream Products

121820-60-8Relevant articles and documents

THERMAL GLYCOSIDATION WITH BENZYLATED GLYCOSYL CHLORIDES: A VERY SIMPLE PROCEDURE FOR O-GLYCOSIDATION

Nishizawa, Mugio,Kan, Yukiko,Yamada, Hidetoshi

, p. 565 - 567 (2007/10/02)

Thermal condensation of benzylated glucosyl chlorides with a variety of alcohols has been achieved efficiently without using any metal salts via a simple operation, and the procedure is used not only for a glucosyl halide, but also for a xylosyl chloride. KEYWORDS O-glycosidation; thermal glycosidation; glucosyl chloride; xylosyl chloride; disaccharide

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