Cas 952688-62-9,3,4-di-O-benzyl-2-deoxy-α-D-glucopyranosyl-(1->5)-3-N-benzoyl-2',3'-O-isopropylidene-uridine

952688-62-9

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Basic information

Product Name: 3,4-di-O-benzyl-2-deoxy-α-D-glucopyranosyl-(1->5)-3-N-benzoyl-2',3'-O-isopropylidene-uridine
Synonyms: 3,4-di-O-benzyl-2-deoxy-α-D-glucopyranosyl-(1->5)-3-N-benzoyl-2',3'-O-isopropylidene-uridine
CAS NO:952688-62-9
Molecular Formula:
Molecular Weight: 714.769
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: 3,4-di-O-benzyl-2-deoxy-α-D-glucopyranosyl-(1->5)-3-N-benzoyl-2',3'-O-isopropylidene-uridine(CAS DataBase Reference)
NIST Chemistry Reference: 3,4-di-O-benzyl-2-deoxy-α-D-glucopyranosyl-(1->5)-3-N-benzoyl-2',3'-O-isopropylidene-uridine(952688-62-9)
EPA Substance Registry System: 3,4-di-O-benzyl-2-deoxy-α-D-glucopyranosyl-(1->5)-3-N-benzoyl-2',3'-O-isopropylidene-uridine(952688-62-9)

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: 952688-62-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 952688-62-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,2,6,8 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 952688-62:
(8*9)+(7*5)+(6*2)+(5*6)+(4*8)+(3*8)+(2*6)+(1*2)=219
219 % 10 = 9
So 952688-62-9 is a valid CAS Registry Number.

952688-62-9Upstream product

952688-62-9Downstream Products

952688-62-9Relevant academic research and scientific papers

Adducts of uridine and glycals as potential substrates for glycosyltransferases

Wandzik, Ilona,Bieg, Tadeusz

, p. 401 - 416 (2007)

We report on the synthesis of 2-deoxyglycosyl derivatives of uridine as potential donor substrates for glycosyltransferases. The totally stereoselective synthesis is accomplished by two sequential addition reactions of uridine derivatives to glycals promo

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