Welcome to LookChem.com Sign In|Join Free

CAS

  • or

167417-45-0

Post Buying Request

167417-45-0 Suppliers

Recommended suppliersmore

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

167417-45-0 Usage

Class

Cyclic amides (lactam)

Molecular Weight

127.14 g/mol

Physical State

White crystalline solid

Solubility

Soluble in water

Applications

Building block in organic compound synthesis
Used in pharmaceutical synthesis
Research and development of new drugs and therapeutic agents

Check Digit Verification of cas no

The CAS Registry Mumber 167417-45-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,4,1 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 167417-45:
(8*1)+(7*6)+(6*7)+(5*4)+(4*1)+(3*7)+(2*4)+(1*5)=150
150 % 10 = 0
So 167417-45-0 is a valid CAS Registry Number.

167417-45-0SDS

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 2-carbamoyl-2-azabicyclo<2.2.1>heptan-3-one

1.2 Other means of identification

Product number -
Other names 3-Oxo-2-aza-bicyclo[2.2.1]heptane-2-carboxylic acid amide

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:167417-45-0 SDS

167417-45-0Downstream Products

167417-45-0Relevant articles and documents

Synthesis of carbocyclic nucleosides from 2-azabicyclo[2.2.1]hept-5-en-3-ones: Sodium borohydride-mediated carbon-nitrogen bond cleavage of five- and six-membered lactams

Katagiri,Muto,Nomura,Higashikawa,Kaneko

, p. 1112 - 1122 (2007/10/02)

Various carbocyclic ribofuranosyl nucleosides were stereoselectively synthesized through a small number of steps from 2-azabicyclo[2.2.1]hept-5-en-3-ones by the use of sodium borohydride-mediated C-N bond cleavage as a key step. Ready availability of a no

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

What can I do for you?
Get Best Price

Get Best Price for 167417-45-0