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103383-72-8

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103383-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103383-72-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,3,8 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 103383-72:
(8*1)+(7*0)+(6*3)+(5*3)+(4*8)+(3*3)+(2*7)+(1*2)=98
98 % 10 = 8
So 103383-72-8 is a valid CAS Registry Number.

103383-72-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(difluoromethyl)-2,4,6-trimethylbenzene

1.2 Other means of identification

Product number -
Other names 2-Difluoromethyl-1,3,5-trimethyl-benzene

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:103383-72-8 SDS

103383-72-8Downstream Products

103383-72-8Relevant articles and documents

gem-Difluoro Compounds: A Convenient Preparation from Ketones and Aldehydes by Halogen Fluoride Treatment of 1,3-Dithiolanes

Sondej, Susan C.,Katzenellenbogen, John A.

, p. 3508 - 3513 (1986)

gem-Difluoro compounds can be prepared from ketones and aldehydes by formation of the corresponding 1,3-dithiolanes, followed by reaction with 1,3-dibromo-5,5-dimethylhydantoin and pyridinium poly(hydrogenfluoride) (HF-pyridine) in methylene chloride.The

Well-Defined, Shelf-Stable (NHC)Ag(CF2H) Complexes for Difluoromethylation

Gu, Yang,Chang, Dalu,Leng, Xuebing,Gu, Yucheng,Shen, Qilong

, p. 3065 - 3071 (2015/06/30)

The preparation of the thermally stable, well-defined NHC-ligated difluoromethylated silver complexes 1a,b is described. The complexes were fully characterized, and the structural assignments were ambiguously further confirmed by single-crystal X-ray diffraction. Reactions of [(SIPr)Ag(CF2H)] with a variety of activated electrophiles such as diaryliodonium salts, vinyl(aryl)iodonium salts, aryldiazonium salts, and acid chlorides in the presence or absence of CuI occurred smoothly at room temperature to generate difluoromethylated compounds in good to excellent yields. (Chemical Equation Presented).

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