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90408-36-9

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90408-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90408-36-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,0 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 90408-36:
(7*9)+(6*0)+(5*4)+(4*0)+(3*8)+(2*3)+(1*6)=119
119 % 10 = 9
So 90408-36-9 is a valid CAS Registry Number.

90408-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (difluoroamino(difluoro)methyl)undecafluorocyclohexane

1.2 Other means of identification

Product number -
Other names [difluoroamino(difluoro)methyl]undecafluorocyclohexane

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:90408-36-9 SDS

90408-36-9Downstream Products

90408-36-9Relevant articles and documents

Reactions of Polyfluorocyclohexane- and Polyfluorocyclohexene-carbonitriles

Phull, Gurjeet S.,Plevey, Raymond G.,Tatlow, John Colin

, p. 455 - 458 (2007/10/02)

The vapour phase reaction of undecafluorocyclohexanecarbonitrile (1) with cobalt(III) or silver(II) fluoride caused stepwise saturation of the CN triple bond to give C6F11CF=NF and C6F11CF2NF2, whereas reaction in a sealed tube with silver(II) fluoride gave the azomethane C6F11CF2N=NCF2C6F11 and with silver(I) fluoride gave tris(undecafluorocyclohexyl)-s-triazine.Methylamine, isopropylamine, and dimethylamine with the nitrile (1) gave the corresponding amidines.Vapour phase fluorination of pentafluorobenzonitrile by cobalt(III) fluoride or potassium tetrafluorocobaltate(III) afforded the nitrile (1), together with nonafluorocyclohex-3-enecarbonitrile (4).The latter was oxidised by potassium permanganate to 3-cyanoheptafluorohexane-1,6-dioic acid.Nonafluorocyclohex-1-enecarbonitrile (2) underwent classical nucleophilic addition-elimination sequences with methanol and with sodium methoxide to give progressively octafluoro-2-methoxy-, heptafluoro-6,6-dimethoxy-, and hexafluoro-2,6,6-trimethoxy-cyclohex-1-enecarbonitrile, whilst with ammonia, 2-aminohexafluoro-6-iminocyclohex-1-enecarbonitrile was formed, again by stepwise addition-elimination.

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