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Acetamide, N-[2-[(phenylmethyl)thio]ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60116-67-8

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60116-67-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60116-67-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,1 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60116-67:
(7*6)+(6*0)+(5*1)+(4*1)+(3*6)+(2*6)+(1*7)=88
88 % 10 = 8
So 60116-67-8 is a valid CAS Registry Number.

60116-67-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-benzylsulfanylethyl)acetamide

1.2 Other means of identification

Product number -
Other names Acetamide,N-[2-[(phenylmethyl)thio]ethyl]

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:60116-67-8 SDS

60116-67-8Relevant academic research and scientific papers

Aqueous metal-free hydrothiolation of enamides and enecarbamates

Barman, Eliezer,Hourezadeh,Lim, Daniel

supporting information, (2019/08/01)

An efficient and metal-free, anti-Markovnikov selective, hydrothioaltion reaction of enamides and enecarbamates in an aqueous medium is presented. This protocol is operationally simple, mild, and atom-economical. This process provides access to thioethers

Metal-free photocatalytic thiol-ene/thiol-yne reactions

Kaur, Sarbjeet,Zhao, Gaoyuan,Busch, Evan,Wang, Ting

supporting information, p. 1955 - 1961 (2019/02/20)

The organic photocatalyst (9-mesityl-10-methylacridinum tetrafluoroborate) in the presence of visible light is used to initiate thiol-ene and thiol-yne reactions. Thiyl radicals are generated upon quenching the photoexcited catalyst with a range of thiols

METHOD FOR MODIFICATION OF ORGANIC MOLECULES

-

Page/Page column 23-25, (2012/12/13)

The present invention is directed to a method of alkylating a thiol group (R-S-H) or seleno group (R-Se-H) in a target molecule wherein the method comprises: reacting a target molecule comprising at least one thiol group with a compound of formula (I) or

A direct method for site-specific protein acetylation

Li, Fupeng,Allahverdi, Abdollah,Yang, Renliang,Lua, Gavian Bing Jia,Zhang, Xiaohong,Cao, Yuan,Korolev, Nikolay,Nordenskioeld, Lars,Liu, Chuan-Fa

supporting information; experimental part, p. 9611 - 9614 (2011/12/05)

Radicals at work: Radical-mediated thiol-ene addition of the thiol group of Cys to N-vinylacetamide gives acetyl-thialysine (KSAc), a near-perfect mimic of acetyl-lysine (see picture). The reaction is highly efficient with near quantitative con

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