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

56986-36-8

Post Buying Request

56986-36-8 Suppliers

Recommended suppliers

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

56986-36-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56986-36-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,8 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56986-36:
(7*5)+(6*6)+(5*9)+(4*8)+(3*6)+(2*3)+(1*6)=178
178 % 10 = 8
So 56986-36-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H14N2O3/c1-3-4-5-9(8-11)6-12-7(2)10/h3-6H2,1-2H3

56986-36-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [butyl(nitroso)amino]methyl acetate

1.2 Other means of identification

Product number -
Other names Butyl acetoxymethylnitrosamine

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:56986-36-8 SDS

56986-36-8Relevant academic research and scientific papers

The Chemistry of Nitrosamines, IV. - Syntheses of α-C-Functionalized N-Nitrosodialkylamines: Esters and Ethers of 1-alcohols

Mueller, Eduard,Kettler, Regina,Wiessler, Manfred

, p. 1468 - 1493 (2007/10/02)

Imines (Schiff's bases) and nitrosyl chloride react to give N-alkyl-1-chloro-N-nitrosoalkylamines 13.Nucleophilic substitution by acetate or p-nitrobenzoate affords the acetates 7 and 9 and p-nitrobenzoates 8 and 10, respectively.The spectroscopic and chemical data of the newly synthesized compounds are discussed.

ISOLATION AND CHARACTERIZATION OF N-ALKYL-N-(HYDROXYMETHYL)NITROSAMINES FROM N-ALKYL-N-(HYDROPEROXYMETHYL)NITROSAMINES BY DEOXYGENATION

Mochizuki, Masataka,Anjo, Takako,Okada, Masashi

, p. 3693 - 3696 (2007/10/02)

N-Alkyl-N-(hydroxymethyl)nitrosamines, postulated intermediates in the metabolic activation of carcinogenic nitrosamines , were prepared by deoxygenation of the corresponding hydroperoxymethyl nitrosamines and characterized

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 56986-36-8