Welcome to LookChem.com Sign In|Join Free
  • or
Acetamide, N-(4-methoxyphenyl)-N-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61667-90-1

Post Buying Request

61667-90-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

61667-90-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61667-90-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,6 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 61667-90:
(7*6)+(6*1)+(5*6)+(4*6)+(3*7)+(2*9)+(1*0)=141
141 % 10 = 1
So 61667-90-1 is a valid CAS Registry Number.

61667-90-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-N-(4-methoxyphenyl)acetamide

1.2 Other means of identification

Product number -
Other names -

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:61667-90-1 SDS

61667-90-1Relevant academic research and scientific papers

A new synthesis of amides and γ-lactones based on the conjugate addition of lithium enolate of amides to 1-chlorovinyl p-tolyl sulfoxides

Satoh, Tsuyoshi,Kamide, Yuhki,Sugiyama, Shimpei

, p. 11805 - 11812 (2007/10/03)

Reaction of 1-chlorovinyl p-tolyl sulfoxides, which were synthesized from chloromethyl p-tolyl sulfoxide and ketones or aldehydes, with lithium enolate of N,N-dimethylacetamide gave the adducts in good to quantitative yields. The adducts were converted to

DIRECT DIACYLATION OF SCHIFF BASES

Vasapollo, Giuseppe,Alper, Howard

, p. 5113 - 5116 (2007/10/02)

A novel diacylation of Schiff bases occurs using catalytic quantities of cobalt carbonyl and phase transfer catalysis conditions.

Bioorganic Studies: Part IV - Reductive N-Acylation of Imines Using 3,5-Dicarbethoxy-2,6-dimethyl-1,4-dihydropyridine as NADH Model

Singh, Serjinder,Sharma, Vijay K.

, p. 1087 - 1088 (2007/10/02)

A one-step reductive acetylation of imines (II) using 3,5-dicarbethoxy-2,6-dimethyl-1,4-dihydropyridine (I) as NADH model is reported.The N-acetyliminium intermediates are reduced in situ by I to give N-acetylamines (IV).Reduction of species which stabili

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 61667-90-1