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6345-81-9

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6345-81-9 Usage

Molecular weight

330.22 g/mol

Functional groups

Trifluoroacetyl, piperazine

Usage

Reagent in the synthesis of pharmaceuticals and agrochemicals

Importance

Key intermediate in the production of various organic compounds

Application

Utilized in the development of new drugs and chemical products

Value

Unique structure and functional groups make it a valuable tool in organic chemistry research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 6345-81-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6345-81:
(6*6)+(5*3)+(4*4)+(3*5)+(2*8)+(1*1)=99
99 % 10 = 9
So 6345-81-9 is a valid CAS Registry Number.

6345-81-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,2-trifluoro-1-[4-(2,2,2-trifluoroacetyl)piperazin-1-yl]ethanone

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:6345-81-9 SDS

6345-81-9Downstream Products

6345-81-9Relevant articles and documents

Ethyl trifluoroacetate: A powerful reagent for differentiating amino groups

Xu, Daqiang,Prasad, Kapa,Repic, Oljan,Blacklock, Thomas J.

, p. 7357 - 7360 (2007/10/02)

Selective protection of primary amines in the presence of secondary amines and monofunctionalization of symmetric primary and secondary diamines using ethyl trifluoroacetate is described. Effective differentiation of primary, secondary and tertiary alkyl-substituted primary amines from one another by ethyl trifluoroacetate acylation is also demonstrated. These results are explained on the basis of steric and electronic effects of the substrate amines.

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