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37169-10-1

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37169-10-1 Usage

General Description

2,4-Dichloro-6-nitrophenyl acetate is a chemical compound with the formula C8H5Cl2NO4. It is a nitrophenyl acetate derivative that is commonly used as a reagent in organic synthesis and chemical research. 2,4-Dichloro-6-nitrophenyl=acetate is a solid, pale yellow in color, and is highly insoluble in water. 2,4-Dichloro-6-nitrophenyl acetate is known for its use as a precursor in the preparation of various pharmaceutical and agrochemical products. It is also utilized in the synthesis of potential bioactive compounds and has been studied for its potential as a pesticide. However, it is important to handle this compound with caution as it can be harmful if ingested or inhaled and may cause skin and eye irritation.

Check Digit Verification of cas no

The CAS Registry Mumber 37169-10-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,1,6 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 37169-10:
(7*3)+(6*7)+(5*1)+(4*6)+(3*9)+(2*1)+(1*0)=121
121 % 10 = 1
So 37169-10-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H5Cl2NO4/c1-4(12)15-8-6(10)2-5(9)3-7(8)11(13)14/h2-3H,1H3

37169-10-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,4-dichloro-6-nitrophenyl) acetate

1.2 Other means of identification

Product number -
Other names 2,4-dichloro-6-nitrophenyl acetate

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:37169-10-1 SDS

37169-10-1Downstream Products

37169-10-1Relevant articles and documents

INTRAMOLECULAR ELECTROPHILIC DISPLACEMENT OF ACYL BY NITRO GROUP DURING ATTEMPTED SYNTHESIS OF 3-NITROCOUMARINS

Benedikt, George M.,Traynor, Lee

, p. 763 - 766 (2007/10/02)

2-Hydroxyacetophenones undergo upon nitration in acetic acid a substitution of the acyl by nitro group followed by an intramolecular 1,3-acyl shift reminescent of a retro-Fries rearrangement to yield phenyl esters.

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