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1-[(4-methoxyphenyl)sulfanyl]-2,4-dinitrobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1871-44-9

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1871-44-9 Usage

Appearance

Yellow crystalline solid

Usage

Reagent in organic synthesis

Usage

Precursor for the production of dyes and pigments

Structural components

Benzene ring

Structural components

Two nitro groups (NO2)

Structural components

Sulfanyl group (S-CH3O)

Functional groups

Nitro groups contribute to reactivity and synthesis potential

Functional groups

Sulfanyl group contributes to reactivity and synthesis potential

Hazard

Toxicity to human health

Hazard

Potential environmental hazards

Precaution

Handle with care due to toxicity and environmental impact

Check Digit Verification of cas no

The CAS Registry Mumber 1871-44-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,7 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1871-44:
(6*1)+(5*8)+(4*7)+(3*1)+(2*4)+(1*4)=89
89 % 10 = 9
So 1871-44-9 is a valid CAS Registry Number.

1871-44-9SDS

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-(4-methoxyphenyl)sulfanyl-2,4-dinitrobenzene

1.2 Other means of identification

Product number -
Other names 1-(2,4-dinitro-phenylsulfanyl)-4-methoxy-benzene

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:1871-44-9 SDS

1871-44-9Relevant academic research and scientific papers

Contribution of linear free energy relationships to isozyme- and pH-dependent substrate selectivity of glutathione S-transferases: Comparison of model studies and enzymatic reactions

Nieslanik, Brenda S.,Atkins, William M.

, p. 6651 - 6660 (1998)

A novel application of linear free energy relationships is described in which the substrate selectivities and pH dependencies of glutathione S-transferases (GSTs) are correlated to the pK(a), of glutathione (GSH) at the active site. To determine whether t

Surfactant-Type Catalyst for Aerobic Oxidative Coupling of Hydrazine with Thiol in Water

Ren, Xuanhe,Tang, Shanyu,Li, Longjia,Li, Jiao,Liang, Helong,Li, Ganzhong,Yang, Guanyu,Li, Heng,Yuan, Bingxin

, p. 8683 - 8690 (2019/07/08)

A series of PEG-functionalized nitrogen ligands were developed to conduct an aerobic oxidative cross-coupling reaction between alkyl- or aryl-hydrazines with thiols in water. This surfactant-type catalyst enables high efficiencies and selectivities, while tolerating a large variety of functional groups. The mother liquor is still catalytically active after five runs.

A highly selective fluorescent probe for thiophenols

Jiang, Wei,Fu, Qingquan,Fan, Hongyou,Ho, Joe,Wang, Wei

, p. 8445 - 8448 (2008/09/19)

A rapid response to thiophenols is obtained with probe 1 (see scheme), which induces a significant (> 50-fold) fluorescence enhancement as a result of cleavage of the electron-withdrawing moiety, thus generating strongly fluorescent molecule 2. No fluores

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