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Benzenesulfenamide, N,N-diethyl-4-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112128-60-6

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112128-60-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112128-60-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,1,2 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 112128-60:
(8*1)+(7*1)+(6*2)+(5*1)+(4*2)+(3*8)+(2*6)+(1*0)=76
76 % 10 = 6
So 112128-60-6 is a valid CAS Registry Number.

112128-60-6SDS

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-ethyl-N-(4-nitrophenyl)sulfanylethanamine

1.2 Other means of identification

Product number -
Other names Benzenesulfenamide,N,N-diethyl-4-nitro

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:112128-60-6 SDS

112128-60-6Relevant academic research and scientific papers

Copper-catalyzed synthesis of sulfenamides utilizing diaryl disulfides with alkyl amines

Taniguchi, Nobukazu

, p. 1917 - 1920 (2008/03/13)

The copper-catalyzed coupling of diaryl disulfides with alkyl amines can afford various sulfenamides in good yields. Furthermore, the present reaction is efficient and can be used for both of the aryl sulfide groups on disulfide. Georg Thieme Verlag Stutt

INVESTIGATION OF THIOSULFONIC ACIDS. XXXIV. REACTION OF THIOSULFONIC ESTERS WITH SULFENAMIDES

Boldyrev, B. G.,Bilozor, T. K.

, p. 1669 - 1671 (2007/10/02)

Thiosulfonic esters react with sulfenamides to form different thiosulfonic esters and sulfenamides.The process is only realized with initial esters having high reactivity and amides having high nucleophilicity, both significantly higher than the analogous characteristics of the final products.

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