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3-Chlorophenyl dimethylcarbamate is a chemical compound with the molecular formula C9H10ClNO2. It is a derivative of phenol, where one hydrogen atom is replaced by a chlorine atom, and the hydroxyl group is converted into a carbamate group. 3-chlorophenyl dimethylcarbamate is an organochlorine pesticide, which was once widely used as an insecticide due to its effectiveness in controlling various pests. However, its use has been restricted or banned in many countries due to concerns about its potential environmental and health impacts, including persistence in the environment, bioaccumulation in the food chain, and toxicity to non-target organisms. The compound is also known for its potential to cause harm to the nervous system and has been classified as a hazardous substance.

7305-02-4

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7305-02-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7305-02-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,0 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7305-02:
(6*7)+(5*3)+(4*0)+(3*5)+(2*0)+(1*2)=74
74 % 10 = 4
So 7305-02-4 is a valid CAS Registry Number.

7305-02-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethyl-butyramide

1.2 Other means of identification

Product number -
Other names Butanamide,N,N-dimethyl

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:7305-02-4 SDS

7305-02-4Relevant academic research and scientific papers

Synthesizing method of multi-aryl substituted naphthol derivate

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Paragraph 0050; 0051; 0052; 0053, (2017/12/27)

The invention discloses a synthesizing method of a multi-aryl substituted naphthol derivate. The method comprises the following steps: performing cyclization reaction on a phenol derivate and a diaromatic acetylene derivate in an organic solvent under the

Pd(II) catalyzed ortho C-H iodination of phenylcarbamates at room temperature using cyclic hypervalent iodine reagents

Sun, Xiuyun,Yao, Xia,Zhang, Chao,Rao, Yu

supporting information, p. 10014 - 10017 (2015/06/22)

A novel approach to access ortho iodinated phenols using cyclic hypervalent iodine reagents through palladium(II) catalyzed C-H activation has been developed through weak coordination. The reaction showed excellent regioselectivity, reactivity and good functional group tolerance. A unique mechanism was proposed.

Room-temperature Pd-catalyzed C-H chlorination by weak coordination: One-pot synthesis of 2-chlorophenols with excellent regioselectivity

Sun, Xiuyun,Sun, Yonghui,Zhang, Chao,Rao, Yu

supporting information, p. 1262 - 1264 (2014/02/14)

A room-temperature Pd(ii)-catalyzed regioselective chlorination reaction has been developed for a facile one-pot synthesis of a broad range of 2-chlorophenols. The reaction demonstrates an excellent regioselectivity and reactivity for C-H chlorination. This reaction represents one of the rare examples of mild C-H functionalization at ambient temperature.

A general approach towards catechol and pyrogallol through ruthenium- and palladium-catalyzed C-H hydroxylation by weak coordination

Yang, Xinglin,Sun, Yonghui,Chen, Zhang,Rao, Yu

supporting information, p. 1625 - 1630 (2014/06/09)

An efficient ruthenium(II)- and palladium(II)-catalyzed C-H hydroxylation of aryl carbamates has been developed for the facile synthesis of catechols and pyrogallols. The reaction demonstrates excellent reactivity, regio- and chemoselectivity, good functional group compatibility and high yields. The practicality of this method has been proved by a gram-scale synthesis.

Palladium catalyzed C-H functionalization of O-arylcarbamates: Selective ortho -bromination using NBS

John, Alex,Nicholas, Kenneth M.

experimental part, p. 5600 - 5605 (2012/07/30)

A series of cyclometalated palladium complexes derived from O-phenylcarbamates has been synthesized by the reaction of the respective carbamates with Pd(OAc)2 in the presence of acids, CF 3CO2H, CF3SO3/sub

Palladium-catalyzed ortho-arylation of O-phenylcarbamates with simple arenes and sodium persulfate

Zhao, Xiaodan,Yeung, Charles S.,Dong, Vy M.

supporting information; experimental part, p. 5837 - 5844 (2010/06/19)

By palladium catalysis, the C-H bond functionalization of O-phenylcarbamates with simple arenes has been achieved using sodium persulfate (Na2S2O8), an inexpensive, easy-to-handle, and environmentally friendly oxidant. Thi

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