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4-(METHYLMERCAPTO)ANILINE HYDROCHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39870-00-3

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39870-00-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39870-00-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,8,7 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 39870-00:
(7*3)+(6*9)+(5*8)+(4*7)+(3*0)+(2*0)+(1*0)=143
143 % 10 = 3
So 39870-00-3 is a valid CAS Registry Number.

39870-00-3SDS

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 4-methylsulfanylaniline,hydrochloride

1.2 Other means of identification

Product number -
Other names 4-(methylmercapto)aniline hydrochloride

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:39870-00-3 SDS

39870-00-3Relevant academic research and scientific papers

Deoxygenation of Nitrous Oxide and Nitro Compounds Using Bis(N-Heterocyclic Silylene)Amido Iron Complexes as Catalysts

Chen, Xi,Driess, Matthias,Du, Shaozhi,Mo, Zhenbo,Wang, Hao

, (2021/12/03)

Herein, we report the efficient degradation of N2O with a well-defined bis(silylene)amido iron complex as catalyst. The deoxygenation of N2O using the iron silanone complex 4 as a catalyst and pinacolborane (HBpin) as a sacrificial reagent proceeds smoothly at 50 °C to form N2, H2, and (pinB)2O. Mechanistic studies suggest that the iron–silicon cooperativity is the key to this catalytic transformation, which involves N2O activation, H atom transfer, H2 release and oxygenation of the boron sites. This approach has been further developed to enable catalytic reductions of nitro compounds, producing amino-boranes with good functional-group tolerance and excellent chemoselectivity.

Syntheses, structures and characterizations of two organoimido derivatives of POMs containing sulfide groups

Guo, Hui,Li, Shang-Ze,Xiong, Xin-Xing,Li, Di,Liu, Zi-Yang,Wang, Long-Sheng,Wu, Ping-Fan

, p. 1 - 6 (2015/04/14)

Two remote methylthio group functionalized organoimido derivatives of hexamolybdate, (Bu4N)2[Mo6O18(NC6H4-SCH3-p)] (1) and (Bu4N)2[Mo6O18/s

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