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96141-37-6

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96141-37-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96141-37-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,1,4 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 96141-37:
(7*9)+(6*6)+(5*1)+(4*4)+(3*1)+(2*3)+(1*7)=136
136 % 10 = 6
So 96141-37-6 is a valid CAS Registry Number.
InChI:InChI=1/C17H17F3N2O5/c18-17(19,20)11-7-22(16(25)21-15(11)24)14-6-12(13(8-23)27-14)26-9-10-4-2-1-3-5-10/h1-5,7,12-14,23H,6,8-9H2,(H,21,24,25)/t12-,13+,14+/m0/s1

96141-37-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3'-O-Benzyl-2'-deoxy-5-(trifluoromethyl)uridine

1.2 Other means of identification

Product number -
Other names 1-O-Benzyl-3-palmitoyl-rac-glycerin

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:96141-37-6 SDS

96141-37-6Downstream Products

96141-37-6Relevant articles and documents

2-deoxyuridines and riboside precursors

-

, (2008/06/13)

A process is provided for the preparation of certain 2-deoxyuridines including the steps forming a substituted alkyl 5-O-"protected"-2-deoxyribofuranoside, hydrocarbylating the latter compound, and condensing the hydrocarbylated compound in the presence o

Studies on antitumor agents. 8. Antitumor activities of O-alkyl derivatives of 2'-deoxy-5-(trifluoromethyl)uridine and 2'-deoxy-5-fluorouridine

Yamashita,Takeda,Matsumoto,Unemi,Yasumoto

, p. 136 - 139 (2007/10/02)

O-Benzyl and O-ethyl derivatives of 2'-deoxy-5-(trifluoromethyl)uridine (F3Thd) and 2'-deoxy-5-fluorouridine (FUdR) were synthesized. The oral antitumor activity of the compounds against sarcoma 180 in mice was examined. The 5'-O-ethyl (3b), 3'

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