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4-NITRO-BENZOIC ACID 2-CHLORO-ETHYL ESTER is an organic compound that features a nitrobenzoic acid group and a 2-chloro-ethyl ester group. It is characterized by its yellow crystalline powder form and is primarily utilized in the synthesis of pharmaceuticals and agrochemicals. Due to its mild irritant properties, it requires careful handling, and proper disposal is necessary to prevent environmental harm.

949-03-1

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949-03-1 Usage

Uses

Used in Pharmaceutical Industry:
4-NITRO-BENZOIC ACID 2-CHLORO-ETHYL ESTER is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs and improve existing ones.
Used in Agrochemical Industry:
4-NITRO-BENZOIC ACID 2-CHLORO-ETHYL ESTER is used as a precursor in the production of agrochemicals, specifically for the creation of pesticides and other crop protection agents, to enhance agricultural productivity and protect crops from pests and diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 949-03-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,4 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 949-03:
(5*9)+(4*4)+(3*9)+(2*0)+(1*3)=91
91 % 10 = 1
So 949-03-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H8ClNO4/c10-5-6-15-9(12)7-1-3-8(4-2-7)11(13)14/h1-4H,5-6H2

949-03-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloroethyl 4-nitrobenzoate

1.2 Other means of identification

Product number -
Other names Monochlorethyl-p-nitrobenzoat

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:949-03-1 SDS

949-03-1Relevant academic research and scientific papers

Transition-metal-free aerobic oxidative cleavage of C-C bonds in α-hydroxy ketones and mechanistic insight to the reaction pathway

Liu, Hui,Dong, Chao,Zhang, Zeguang,Wu, Peiyu,Jiang, Xuefeng

supporting information, p. 12570 - 12574 (2013/02/22)

Clear cut: For the title reaction, O2, the ideal oxidant, was used as the only oxidizing reagent. The dimer intermediate (see scheme) and isotopic labeling control experiments with 18O2 partially disclosed the reaction mec

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