Basic information

Product Name: Cytidine, N-acetyl-, 2',3',5'-tribenzoate
Synonyms:
CAS NO:27391-03-3
Molecular Formula: C32H27N3O9
Molecular Weight: 597.581
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: Cytidine, N-acetyl-, 2',3',5'-tribenzoate(CAS DataBase Reference)
NIST Chemistry Reference: Cytidine, N-acetyl-, 2',3',5'-tribenzoate(27391-03-3)
EPA Substance Registry System: Cytidine, N-acetyl-, 2',3',5'-tribenzoate(27391-03-3)

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: 27391-03-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 27391-03-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,3,9 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 27391-03:
(7*2)+(6*7)+(5*3)+(4*9)+(3*1)+(2*0)+(1*3)=113
113 % 10 = 3
So 27391-03-3 is a valid CAS Registry Number.

27391-03-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	N4-acetyl-O2',O3',O5'-tribenzoyl-cytidine

1.2 Other means of identification

Product number	-
Other names	4-N-Acetyl-2',3',5'-tri-O-benzoylcytidin

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:27391-03-3 SDS

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27391-03-3Relevant academic research and scientific papers

Glycosyl iodides. History and recent advances

Meloncelli, Peter J.,Martin, Alan D.,Lowary, Todd L.

, p. 1110 - 1122 (2009)

The use of glycosyl iodides as an effective method for the preparation of glycosides has had a recent resurgence in carbohydrate chemistry, despite its early roots in which these species were believed to be of limited use. Renewed interest in these specie

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