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2-chloro-5-nitrobenzenesulphinic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61886-18-8

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61886-18-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61886-18-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,8,8 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61886-18:
(7*6)+(6*1)+(5*8)+(4*8)+(3*6)+(2*1)+(1*8)=148
148 % 10 = 8
So 61886-18-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H4ClNO4S/c7-5-2-1-4(8(9)10)3-6(5)13(11)12/h1-3H,(H,11,12)

61886-18-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-5-nitrobenzenesulfinic acid

1.2 Other means of identification

Product number -
Other names 2-chloro-5-nitrobenzenesulphinic acid

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:61886-18-8 SDS

61886-18-8Relevant academic research and scientific papers

Dye intermediate (3-beta-hydroxyethylsulfonyl)aniline-4-aminoacetic acid and preparation method thereof

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, (2017/02/28)

The invention relates to a dye intermediate (3-beta-hydroxyethylsulfonyl)aniline-4-aminoacetic acid and a preparation method thereof. The dye intermediate, (3-beta-hydroxyethylsulfonyl)aniline-4-aminoacetic acid, is represented as the structure formula (I). The preparation method includes the steps of: chlorosulfonation of 2-chloro-5-nitrobenzenesulfonic acid, reduction by sodium sulfite, hydroxyethylation, a condensation reaction with aminoacetic acid, hydrogenation reduction of the nitro group, and the like. The novel dye intermediate, compared with common dye intermediates, can greatly improve the water solubility of a dye, and reduces production cost and reduces environment pollution.

Nitrodiaryl sulfoxide derivatives, process for their preparation and pharmaceutical and pesticidal compositions containing them as active ingredient

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, (2008/06/13)

The invention relates to a new process for the preparation of aminodiaryl sulfoxide derivatives of the formula (I), STR1 wherein X is halogen, alkoxy having from 1 to 6 carbon atoms or a group --(N,R,R1), in which R and R1 are hydrogen or alkyl having from 1 to 6 carbon atoms, R2 is hydrogen, halogen, alkyl having from 1 to 6 carbon atoms, alkoxy having from 1 to 6 carbon atoms or phenyl or phenylthio both optionally substituted by one or more identical or different halogen(s) and/or amino group(s), and acid addition salts thereof. The compounds of formula (I) are pharmaceutically active, in particular are potent anthelmintics, or can be used as active ingredients in pesticidal compositions. The invention therefore relates to pharmaceutical and pesticidal compositions containing compounds of formula (I) or salts thereof as active ingredient. Compounds of formula (I), in which the substituents are as defined above, but if X stands for a group --N(R,R1) in which R and R1 both represent hydrogen, and X is in para-position related to the sulfoxide group, then R2 is other than hydrogen, halogen, alkyl having from 1 to 6 carbon atoms and alkoxy having from 1 to 6 carbon atoms, and the acid addition salts thereof, are new. These new compounds are also subject of the present invention.

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