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74032-55-6

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74032-55-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74032-55-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,0,3 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 74032-55:
(7*7)+(6*4)+(5*0)+(4*3)+(3*2)+(2*5)+(1*5)=106
106 % 10 = 6
So 74032-55-6 is a valid CAS Registry Number.

74032-55-6SDS

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 trans-perfluoro-4-methyl-2-pentenedinitrile

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:74032-55-6 SDS

74032-55-6Upstream product

74032-55-6Downstream Products

74032-55-6Relevant articles and documents

IONIC DIMERISATION OF TRIFLUOROPROPENENITRILE AND ITS ADDITION REACTIONS WITH METHYL TRIFLUOROPROPENOATE

Svoboda, Jiri,Paleta, Oldrich,Dedek, Vaclav

, p. 406 - 414 (2007/10/02)

Dimerisation of trifluoropropenenitrile (I) in the presence of potassium fluoride and tertiary amines afforded a mixture of stereoisomeric perfluoro-4-methyl-2-pentenedinitriles (II), higherboiling compounds, and 2,3,3,3-tetrafluoropropanenitrile (III) which arises by proton transfer from the solvent molecule.Under optimum conditions, product II was obtained in about 50percent yield.Reaction of the nitrile I with methyl trifluoropropenoate (IV) gave, besides the dimers II and V, the product of addition of the nitrile I to the propenoate, IV, i.e. methyl 4-cyanoperfluoro-2-pentenoate (VI), and the addition product of the propenoate IV to the nitrile I, i.e. methyl 4-cyanoperfluoro-2-methyl-3-butenoate (VII).The relative reactivity of I and IV is discussed.The ratio of stereoisomers in II, V, VI and VII indicates that the magnitude of the steric substituent effect, operating in the reaction mechanism, decreases in the order -CFCF3(COOCH3)> -CFCF3(CN)> -COOCH3> -CN.

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