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110225-41-7

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110225-41-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110225-41-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,2,2 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 110225-41:
(8*1)+(7*1)+(6*0)+(5*2)+(4*2)+(3*5)+(2*4)+(1*1)=57
57 % 10 = 7
So 110225-41-7 is a valid CAS Registry Number.

110225-41-7SDS

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 1,3-dimethyl-6-(2,5-dimethylphenyl)uracil

1.2 Other means of identification

Product number -
Other names -

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:110225-41-7 SDS

110225-41-7Downstream Products

110225-41-7Relevant articles and documents

Palladium-catalyzed direct 5-arylation of 1,3-dimethyluracil with aryl bromides: An electrophilic metalation-deprotonation with electrophilic arylpalladium intermediate

Kim, Ko Hoon,Lee, Hyun Seung,Kim, Jae Nyoung

scheme or table, p. 6228 - 6233 (2011/12/14)

An efficient method of palladium-catalyzed direct 5-arylation of 1,3-dimethyluracil was developed with a various range of aryl bromides including electron-deficient aryl bromides. 5-Aryluracil derivatives were obtained in moderate to good yields regiosele

Photolysis of 5-bromo-1,3-dimethyluracil in substituted benzenes

Seki,Matsuda,Bando,Ohkura

, p. 4737 - 4748 (2007/10/02)

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PHOTOLYSIS OF 5-BROMO-1,3-DIMETHYLURACIL IN SUBSTITUTED BENZENES

Seki, Koh-ichi,Bando, Yuko,Ohkura, Kazue

, p. 195 - 196 (2007/10/02)

Photolysis of 5-bromo-1,3-dimethyluracyl in toluene, xylene and anisole afforded the anormalously substituted 6-aryl-1,3-dimethyluracils beside the expected products 5-aryl-1,3-dimethyluracils, while the reaction with veratrole occured exclusively at the 5-position of the uracil ring.

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