Cas 1615710-98-9,3-O-[4-O-benzyl-2,3,6-trideoxy-β-L-threo-hex-2-enopyranosyl]-1,5-anhydro-4-O-benzyl-2,6-dideoxy-L-lyxo-hex-1-enitol

1615710-98-9

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Basic information

Product Name: 3-O-[4-O-benzyl-2,3,6-trideoxy-β-L-threo-hex-2-enopyranosyl]-1,5-anhydro-4-O-benzyl-2,6-dideoxy-L-lyxo-hex-1-enitol
Synonyms: 3-O-[4-O-benzyl-2,3,6-trideoxy-β-L-threo-hex-2-enopyranosyl]-1,5-anhydro-4-O-benzyl-2,6-dideoxy-L-lyxo-hex-1-enitol
CAS NO:1615710-98-9
Molecular Formula:
Molecular Weight: 422.521
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: 3-O-[4-O-benzyl-2,3,6-trideoxy-β-L-threo-hex-2-enopyranosyl]-1,5-anhydro-4-O-benzyl-2,6-dideoxy-L-lyxo-hex-1-enitol(CAS DataBase Reference)
NIST Chemistry Reference: 3-O-[4-O-benzyl-2,3,6-trideoxy-β-L-threo-hex-2-enopyranosyl]-1,5-anhydro-4-O-benzyl-2,6-dideoxy-L-lyxo-hex-1-enitol(1615710-98-9)
EPA Substance Registry System: 3-O-[4-O-benzyl-2,3,6-trideoxy-β-L-threo-hex-2-enopyranosyl]-1,5-anhydro-4-O-benzyl-2,6-dideoxy-L-lyxo-hex-1-enitol(1615710-98-9)

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: 1615710-98-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1615710-98-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,5,7,1 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1615710-98:
(9*1)+(8*6)+(7*1)+(6*5)+(5*7)+(4*1)+(3*0)+(2*9)+(1*8)=159
159 % 10 = 9
So 1615710-98-9 is a valid CAS Registry Number.

1615710-98-9Upstream product

137035-65-5 1,5-anhydro-4-O-benzyl-2,6-dideoxy-L-lyxo-hex-1-enitol

1615710-98-9Downstream Products

1615710-98-9Relevant academic research and scientific papers

An approach for disaccharide chiron synthesis using a Ferrier-type rearrangement

Komor, Katarzyna,Szeja, Wies?aw,Bieg, Tadeusz,Ku?nik, Nikodem,Pastuch-Gawo?ek, Gabriela,Komor, Roman

, p. 3709 - 3712 (2014)

We report a new approach for the synthesis of new chiral synthons in which two unsaturated sugars are linked via a glycosidic bond. The di-unsaturated disaccharide can be further functionalized using effective, highly selective methods and used in convergent syntheses of relatively complex glycoconjugates. Our approach utilizes in situ generation of active glycosyl donors via Ferrier-type rearrangement under phase-transfer conditions and subsequent reaction with a nucleophile.

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