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89639-95-2

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89639-95-2 Usage

Physical state

Yellow to brown liquid

Uses

Production of dyes, pharmaceuticals, and agricultural chemicals

Odor

Strong

Toxicity

Toxic if ingested or inhaled

Hazardous properties

Skin and eye irritant

Safety precautions

Handled and stored with appropriate safety measures to avoid human and environmental exposure

Check Digit Verification of cas no

The CAS Registry Mumber 89639-95-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,6,3 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 89639-95:
(7*8)+(6*9)+(5*6)+(4*3)+(3*9)+(2*9)+(1*5)=202
202 % 10 = 2
So 89639-95-2 is a valid CAS Registry Number.

89639-95-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(chloromethylsulfanyl)-2-nitrobenzene

1.2 Other means of identification

Product number -
Other names 2-nitrophenyl chloromethyl sulfide

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:89639-95-2 SDS

89639-95-2Downstream Products

89639-95-2Relevant articles and documents

SYNTHESIS AND CONFIGURATIONAL STUDIES OF ARYL CYCLOPROPYL SULFONES

Reddy, D. Bhaskar,Balaji, T.,Reddy, B. Venkataramana

, p. 297 - 306 (2007/10/02)

The cycloaddition of arylthiocarbenes to styrene gave stereospecifically cis-1-(arylthio)-2-phenylcyclopropanes, which were subsequently oxidized to the corresponding sulfones.The cyclopropanation of α,β-unsaturated sulfones with dimethylsulfonium methylide yielded stereoselectively trans-1-(arylsulfonyl)-2-arylcyclopropanes.The configurational assignments of these compounds have been arrived at on the basis of IR and PMR spectral data.Chemical shifts for ring protons and other substituents reveal that all the substituents tend to cause protons cis to them to appear at higher fields than those trans to them.This has been used as a criterion to distinguish between cis and trans aryl cyclopropyl sulfones.

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