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FENTRAZAMIDE METABOLITE 1 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

98377-35-6

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98377-35-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98377-35-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,3,7 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 98377-35:
(7*9)+(6*8)+(5*3)+(4*7)+(3*7)+(2*3)+(1*5)=186
186 % 10 = 6
So 98377-35-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H5ClN4O/c8-5-3-1-2-4-6(5)12-7(13)9-10-11-12/h1-4H,(H,9,11,13)

98377-35-6 Well-known Company Product Price

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  • Sigma-Aldrich

  • (33951)  FentrazamideMetabolitesolution  100 μg/mL in acetonitrile, PESTANAL®, analytical standard

  • 98377-35-6

  • 33951-2ML-R

  • 629.46CNY

  • Detail

98377-35-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-chlorophenyl)-2H-tetrazol-5-one

1.2 Other means of identification

Product number -
Other names 1-(2-Chlorophenyl)-1,4-dihydro-5-tetrazolone

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:98377-35-6 SDS

98377-35-6Relevant academic research and scientific papers

Reactions of dimethyl 2-chloroethynylphosphonate with 1-substituted 5-oxo-1H-1,2,3,4-tetrazoles

Mel'nikova,Myznikov,Dogadina,Svintsitskaya

, p. 2160 - 2166 (2015/02/02)

Addition of 1-substituted tetrazol-5-ones to dimethyl 2-chloroethynylphosphonate occurred regioselectively to form new geminally substituted bis(4-R-5-oxo-4,5-dihydro-1H-tetrazol-1-yl)ethenylphosphonates with 65- 92% yield.

Process for the preparation of 1-4-disubstituted-5 (4H)-tetrazolinones

-

, (2008/06/13)

1,4-Disubstituted-5(4H)-tetrazolinones of the formula (I) STR1 wherein R1, R2 and R3 have the meanings given in the specification), which are known to be useful as herbicides, can be obtained in very good yields by reacting the corresponding 1-substituted-5(4H)-tetrazolinones with the corresponding carbamoyl chlorides in the presence of 4-dimethylaminopyridine.

Process for producing 1-(2-chlorophenyl)-5(4H)-tetrazolinone

-

, (2008/06/13)

STR1 The intermediate is new. The reactions are also new and may be effected separately or as a one-pot process without isolation or purification of the intermediate.

Herbicidally active tetrazolinones

-

, (2008/06/13)

Selective herbicidal tetrazolinones of the formula STR1 wherein X is hydrogen or halogen, Y is hydrogen or C1-4 alkyl, R1 is C1-4 alkyl, and R2 is cycloheptyl or cyclooctyl. and synergistic mixtures thereof.

Process for the production of 1-substituted-5(4H)-tetrazolinones

-

, (2008/06/13)

1-Substituted-5(4H)-tetrazolinones of the formula (I) STR1 wherein R is alkyl, haloalkyl, cycloalkyl, phenyl, substituted phenyl or aralkyl, are obtained in very good yields by reacting, in a polar solvent, an isocyanate of the formula R-NCO (II) with sod

Process for the preparation of 1-substituted-5(4H)-tetrazolinones

-

, (2008/06/13)

A process for the preparation of a 1-substituted-5(4H)-tetrazolinone of the formula STR1 wherein R1 is defined in the specification n is 0, 1, 2, 3 or 4, which comprises reacting a 1-substituted-5(4H)-tetrazolinethione of the formula STR2 with an ethylene oxide of the formula STR3 wherein R2 represents hydrogen, methyl or ethyl, in the presence of a base and in the presence of water, an alcohol or a mixture thereof.

Tetrzolinone herbicides

-

, (2008/06/13)

Novel tetrazolinones of the formula (I) STR1 wherein X is chlorine or bromine, Y is hydrogen, chlorine, bromine, methyl or ethyl, and R1 and R2 are the same or different C2-4 alkyl, a process for their preparation, and the use of the new compounds as herbicides, especially against paddy-weeds.

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