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2,4(1H,3H)-Pyrimidinedione, 1-(diphenylmethyl)-5-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

696617-65-9

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696617-65-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 696617-65-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,6,6,1 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 696617-65:
(8*6)+(7*9)+(6*6)+(5*6)+(4*1)+(3*7)+(2*6)+(1*5)=219
219 % 10 = 9
So 696617-65-9 is a valid CAS Registry Number.

696617-65-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzhydryl-5-methylpyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 1-benzhydryl-5-methyl-1H-pyrimidine-2,4-dione

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:696617-65-9 SDS

696617-65-9Relevant academic research and scientific papers

Regioselective synthesis of 1-allyl- and 1-arylmethyl uracil and thymine derivatives

Malik, Vaishali,Singh, Palwinder,Kumar, Subodh

, p. 4009 - 4014 (2007/10/03)

2,4-Bis(trimethylsiloxy) pyrimidines 1 with allyl halides and arylmethyl halides in 1,2-dichloroethane in the presence of I2 regioselectively provide 1-allyl-/1-arylmethyl-uracil and thymine derivatives. The secondary aryl alkyl and diaryl meth

Benzhydryl as an efficient selective nitrogen protecting group for uracils

Wu, Fan,Buhendwa, Musole G.,Weaver, Donald F.

, p. 9307 - 9309 (2007/10/03)

Regioselective N-substitution of the less active nitrogen within uracil analogues has been achieved following preliminary N-protection at the more active N-position with a benzhydryl protecting group. This protecting group is stable to concentrated HCl (a

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