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Bicyclo[2.2.1]heptane-2,5-diamine, (1R,2R,4R,5R)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

698353-43-4

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698353-43-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 698353-43-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,8,3,5 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 698353-43:
(8*6)+(7*9)+(6*8)+(5*3)+(4*5)+(3*3)+(2*4)+(1*3)=214
214 % 10 = 4
So 698353-43-4 is a valid CAS Registry Number.

698353-43-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,4R)-DIANANE

1.2 Other means of identification

Product number -
Other names (1R,2R,4R,5R)-2,5-diaminobicyclo[2.2.1]heptane

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:698353-43-4 SDS

698353-43-4Relevant academic research and scientific papers

Enantioselective Synthesis of DIANANE, a Novel C2-Symmetric Chiral Diamine for Asymmetric Catalysis

Berkessel, Albrecht,Schroeder, Michael,Sklorz, Christoph A.,Tabanella, Stefania,Vogl, Nadine,Lex, Johann,Neudoerfl, Joerg M.

, p. 3050 - 3056 (2007/10/03)

DIANANE (endo,endo-2,5-diaminonorbornane) is a novel chiral C 2-symmetric diamine, based on the rigid bicyclo[2.2.1]heptane scaffold. Schiff-base ligands derived from DIANANE have already found use in asymmetric catalysis, e.g., in the highly e

A highly enantioselective catalyst for the asymmetric Nozaki-Hiyama-Kishi reaction of allylic and vinylic halides

Berkessel, Albrecht,Menche, Dirk,Sklorz, Christoph A.,Schroeder, Michael,Paterson, Ian

, p. 1032 - 1035 (2007/10/03)

Catalytic asymmetric addition of vinylic halides and trifiates to aldehydes, with useful levels of stereoinduction, has been achieved for the first time using the salentype ligand (S,S)-5 (see scheme; PMB=para-methoxybenzyl), which contains the novel endo

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