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1-Propanone, 1-(2-methyl-6-phenyl-4-pyrimidinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74502-90-2

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74502-90-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74502-90-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,5,0 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 74502-90:
(7*7)+(6*4)+(5*5)+(4*0)+(3*2)+(2*9)+(1*0)=122
122 % 10 = 2
So 74502-90-2 is a valid CAS Registry Number.

74502-90-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-methyl-6-phenylpyrimidin-4-yl)propan-1-one

1.2 Other means of identification

Product number -
Other names ethyl 2-methyl-6-phenyl-4-pyrimidinyl ketone

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:74502-90-2 SDS

74502-90-2Downstream Products

74502-90-2Relevant academic research and scientific papers

Studies on Pyrimidine Derivatives. XXXIII. Synthesis of Alkyl Pyrimidinyl Ketones by Means of Nitrosation of Alkylpyrimidines

Sakamoto, Takao,Sakasai, Takeji,Yoshizawa, Hiroshi,Tanji, Ken-Ichi,Nishimura, Sumiko,Yamanaka, Hiroshi

, p. 4554 - 4560 (2007/10/02)

The reaction of 4-alkylpyrimidines with propyl nitrite under acidic conditions followed by deoximation of the resulting ketoximes gave alkyl pyrimidinyl ketones in satisfactory yields.As compared with the direct oxidation of the alkylpyrimidines with sele

Studies on Pyrimidine Derivatives. XV. Homolytic Acylation and Amidation of Simply Substituted Pyrimidines

Sakamoto, Takao,Ono, Takayasu,Sakasai, Takeji,Yamanaka, Hiroshi

, p. 202 - 207 (2007/10/02)

The reaction of 2,6-disubstituted pyrimidines with acyl radicals generated either from pyruvic acid-AgNO3-(NH4)2S2O8 ( method A ) or from aldehyde-FeSO4-t-BuOOH ( method B ) in aq.H2SO4, gave the corresponding 2,6-disubstituted 4-acylpyrimidines.However,

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