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36918-79-3

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36918-79-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36918-79-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,9,1 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 36918-79:
(7*3)+(6*6)+(5*9)+(4*1)+(3*8)+(2*7)+(1*9)=153
153 % 10 = 3
So 36918-79-3 is a valid CAS Registry Number.

36918-79-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-nitro-N-(1H-1,2,4-triazol-5-yl)benzamide

1.2 Other means of identification

Product number -
Other names T0501-0713

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:36918-79-3 SDS

36918-79-3Downstream Products

36918-79-3Relevant articles and documents

Triazole-containing compounds of structure and its preparation method and use as herbicides

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Paragraph 0092; 0093, (2016/12/07)

The invention discloses a compound comprising a triazole structure, a preparation method thereof and an application of the compound taken as a weed killer. The structure formula of the compound comprising the triazole structure is shown in a formula I, R represents allyl, alkyl acyl with a carbon atom number of 1-20, substituted or un-substituted benzoyl, O, O-dimethyl phosphoroamido-thioate, phenyl, benzene oxygen acetyl, 3-phenyl-2 acryl or 2, 6-binitro-4-trifluoro methyl phenyl. The preparation method of the compound shown in the formula I comprises the steps as follows: under the catalytic action of alkali, 3-amino-1 H-1, 2, 4-triazole and an electrophilic reagent are subjected to electrophilic substitution reaction, so that the compound shown in the formula I is obtained. The weed killer can be used for preventing and killing weeds, green bristle grass, crab grass, eleusine indica, black nightshade, amaranth, piemarker, quinoa, scandent hop, summer cypress, field bindweed, acalypha australis, Ixeris chinensis and viola prionantha.

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