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19455-20-0

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19455-20-0 Usage

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 19455-20-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,5 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19455-20:
(7*1)+(6*9)+(5*4)+(4*5)+(3*5)+(2*2)+(1*0)=120
120 % 10 = 0
So 19455-20-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H8O2.K/c1-3(2)4(5)6;/h3H,1-2H3,(H,5,6);/q;+1/p-1

19455-20-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name potassium,2-methylpropanoate

1.2 Other means of identification

Product number -
Other names ACMC-209eyc

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:19455-20-0 SDS

19455-20-0Relevant articles and documents

Utilising 14C-radiolabelled atom transfer radical polymerisation initiators

Long, Mark,Thornthwaite, David W.,Rogers, Suzanne H.,Bonzi, Gwenaelle,Livens, Francis R.,Rannard, Steve P.

supporting information; experimental part, p. 6406 - 6408 (2010/03/04)

14C-radio-initiated atom transfer radical polymerisations allow direct monitoring of the fate of initiating species.

Isolation of Crystalline Potassium Alkanecarboselenoates

Kageyama, Hideki,Takagi, Kazutaka,Murai, Toshiaki,Kato, Shinzi

, p. 1519 - 1523 (2007/10/02)

A series of potassium alkanecarboselenoates (2) were isolated as crystals from the reaction of the corresponding bis(acyl)selenides with potassium methanolate.The salts 2 readily react with alkyl iodides at 0 deg C to afford the corresponding alkyl alkanecarboselenoates (3) in quantitative yields. - Key words: Potassium Alkanecarboselenoates, Potassium Selenocarboxylate, Selenocarboxylic Acid Potassium Salts

N,N-dialkyl-N'-(substituted-5-isothioazolyl)-N'-acylureas as herbicides

-

, (2008/06/13)

A new class of herbicidal compounds consisting of N,N-dialkyl-N'-(substituted-5-isothiazolyl)-N'-acylureas in which the 3-substitutent on the isothioazole moiety consists of alkyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, and dialkylamino, and the 4-substituent on the isothiazole moiety consists of cyano, alkoxycarbonyl, and nitro; and in which the nitrogen atom of the N,N-dialkylurea to which the isothiazolyl moiety is bonded, is also bonded to an acyl moiety, exhibits outstanding preemergence and postemergence herbicidal activity, controlling effectively the growth of a wide spectrum of grassy and broad-leaved plant species. The synthesis of members of this class is described in detail and the utility of representative compounds is exemplified.

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