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82407-82-7

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82407-82-7 Usage

Abbreviation

TBD

Type of compound

Bicyclic amine

Structure

Rigid, cage-like

Steric hindrance

High

Basicity

High

Role

Catalyst in chemical reactions

Applications

a. Transesterification of esters
b. Synthesis of peptides and oligonucleotides
c. Formation of carbon-carbon bonds

Selectivity

Able to selectively catalyze certain reactions and minimize unwanted side products

Deprotonation

Efficiently and selectively deprotonates weak acids

Importance

Essential reagent for organic chemists and an important tool in modern organic synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 82407-82-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,4,0 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 82407-82:
(7*8)+(6*2)+(5*4)+(4*0)+(3*7)+(2*8)+(1*2)=127
127 % 10 = 7
So 82407-82-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H24N2/c1-2-4-8-14-11-5-9-13(7-3-1)10-6-12-14/h1-12H2

82407-82-7SDS

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 1,8-diazabicyclo[6.3.3]tetradecane

1.2 Other means of identification

Product number -
Other names 1,5-Diazabicyclo<6.3.3>tetradecane

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:82407-82-7 SDS

82407-82-7Upstream product

82407-82-7Downstream Products

82407-82-7Relevant articles and documents

SYNTHESIS OF MEDIUM-RING BICYCLIC DIAMINES BY THE ALKYLATION AND CLEAVAGE OF CYCLIC AMIDINES

Alder, Roger W.,Sessions, Richard B.

, p. 1121 - 1124 (1982)

1,6-Diazabicyclododecane (7), 1,6-diazabicycloundecane (8) and 1,8-diazabicyclotridecane (9) have been made by reduction of tricyclic α-aminoammonium salts with LiAlH4; the protonation and oxidation of 8 and 9 are discussed.

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