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Benzenemethanol, 4-methoxy-a-(4-methoxyphenyl)-a-(trichloromethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61698-78-0

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61698-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61698-78-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,9 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61698-78:
(7*6)+(6*1)+(5*6)+(4*9)+(3*8)+(2*7)+(1*8)=160
160 % 10 = 0
So 61698-78-0 is a valid CAS Registry Number.

61698-78-0SDS

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 1,1-dianisyl-2,2,2-trichloroethanol

1.2 Other means of identification

Product number -
Other names mono-hydroxymethoxychlor

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:61698-78-0 SDS

61698-78-0Relevant academic research and scientific papers

1,1-Dianisyl-2,2,2-trichloroethyl ethers - A new protection for the hydroxyl group

Karl,Kloesel, Rosa Maria KarlRoland,Klosel,Koenig, Stephan,Konig,Lehnhoff, Stefan,Lehnhoff,Ugi, Ivar,Ugi

, p. 3759 - 3766 (2007/10/02)

β-Haloalkyl protecting groups are well established. However, there was a lack of an appropriate protection, especially for carboxyl and vicinal hydroxyl groups. This problem was now solved by design of the 1,1-dianisyl-2,2,2-trichloroethyl group (DATE). The alkylation of model alcohols with the DATE moiety is described. The resulting β-haloalkyl ethers proved to be remarkable stable against acids and bases. Deblocking of the model alcohols is achieved in high yields.

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