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85743-99-3

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85743-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85743-99-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,7,4 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 85743-99:
(7*8)+(6*5)+(5*7)+(4*4)+(3*3)+(2*9)+(1*9)=173
173 % 10 = 3
So 85743-99-3 is a valid CAS Registry Number.

85743-99-3SDS

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 N-(2-trimethylsilyloxypyrimidin-4-yl)benzamide

1.2 Other means of identification

Product number -
Other names Benzamide,N-[2-[(trimethylsilyl)oxy]-4-pyrimidinyl]

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:85743-99-3 SDS

85743-99-3Relevant articles and documents

A key intermediate for the preparation of rope non-cloth wei (by machine translation)

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Paragraph 0028; 0035; 0042, (2019/04/02)

The invention relates to a kind of the formula (I): As shown by a rope non-cloth wei key intermediate of the preparation method, the present invention in order to compound 3, 5 - dibenzoyl - 2 - deoxy - 2 - fluoro - 2 methyl - D - ribose - γ - lactone as

Β-selective D-psicofuranosylation of pyrimidine bases and thiols

Ueda, Atsushi,Nishimura, Yuri,Makura, Yui,Tanaka, Masakazu,Uenishi, Junichi

, p. 729 - 743 (2019/04/26)

N-Glycosidation of D-psicofuranosyl donor 1 with pyrimidine bases took place β-selectively in a β/α-ratio of 8:1 ~ 7:1. For S-glycosidation, 3,4-O-(3-pentylidene)-protected D-psicofuranosyl donor 15 was effective to increase β-selectivity up to 7:1.

PROCESS FOR THE PREPARATION OF SOFOSBUVIR

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Page/Page column 26, (2017/06/09)

A process for the preparation of intermediates 9, useful in the synthesis of sofosbuvir, as well as intermediates of formula [12] are disclosed herein.

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