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29723-29-3

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29723-29-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29723-29-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,7,2 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 29723-29:
(7*2)+(6*9)+(5*7)+(4*2)+(3*3)+(2*2)+(1*9)=133
133 % 10 = 3
So 29723-29-3 is a valid CAS Registry Number.

29723-29-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,3,3,4,4,4-heptafluoro-N-(2-phenylethyl)butanamide

1.2 Other means of identification

Product number -
Other names N-Phenaethyl-heptafluorbutyramid

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:29723-29-3 SDS

29723-29-3Downstream Products

29723-29-3Relevant articles and documents

Overcoming inaccessibility of fluorinated imines-synthesis of functionalized amines from readily available fluoroacetamides

Czerwiński, Pawe? J.,Furman, Bart?omiej

supporting information, p. 9436 - 9439 (2019/08/15)

Although imines are convenient substrates for the synthesis of functionalized amines, they may be hard to obtain, as in the case of fluorinated imines. To aid in overcoming this issue, we propose a protocol of corresponding amine synthesis from simple fluoroacetic acid-derived amides using Schwartz's reagent.

1(Or 3)-perfluoroalkyl-3,4-dihydro-2(1H)-isoquinolinecarbonitriles

-

, (2008/06/13)

(1-R- or 3-trifluoromethyl)-3,4-dihydro-2(1H)-isoquinolinecarboxamidoximes where R is pentafluoroethyl or heptafluoropropyl, having antithrombotic and antibacterial activities, are prepared by reacting the corresponding (1-R- or 3-trifluoromethyl)-3,4-dih

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