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Bicyclo[2.2.1]heptan-2-amine, 1,7,7-trimethyl-, (1R,2R,4R)-rel- is a complex organic compound with the molecular formula C10H19N. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it exists in the (1R,2R,4R)-rel configuration. Bicyclo[2.2.1]heptan-2-amine,1,7,7-trimethyl-, (1R,2R,4R)-rel- is characterized by its bicyclic structure, with two carbon rings fused together, and an amine functional group attached to the second carbon of the bicyclic structure. The presence of three methyl groups at the 1st, 7th, and 7th positions (with the last being a repetition due to the structure's symmetry) adds to its complexity. Bicyclo[2.2.1]heptan-2-amine,1,7,7-trimethyl-, (1R,2R,4R)-rel- is of interest in organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other specialty chemicals.

2223-67-8

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2223-67-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2223-67-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,2 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2223-67:
(6*2)+(5*2)+(4*2)+(3*3)+(2*6)+(1*7)=58
58 % 10 = 8
So 2223-67-8 is a valid CAS Registry Number.

2223-67-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,7,7-trimethylbicyclo[2.2.1]heptan-exo-2-amine

1.2 Other means of identification

Product number -
Other names Bicyclo[2.2.1]heptan-2-amine, 1,7,7-trimethyl-, exo-

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:2223-67-8 SDS

2223-67-8Relevant academic research and scientific papers

EPIMERIZATION OF ENDO- AND EXO-BORNEOLS IN THE PRESENCE OF AMMONIA AND/OR HYDROGEN ON A FUSED IRON CATALYST

Glebov, L. S.,Shuikin, A. N.,Kliger, G. A.,Loktev, S. M.

, p. 1985 - 1987 (1990)

Epimerization of borneols was noted upon their reaction with ammonia and/or hydrogen on fused iron catalyst.Borneols are hydroaminated to give bornylamines with predominance of the endo isomer.

CYANO-PYRIMIDINE INHIBITORS OF EGFR/HER2

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Page/Page column 58-59, (2021/07/17)

Provided herein are compounds, pharmaceutical compositions comprising such compounds, and methods of using such compounds to treat diseases or disorders associated with EGFR and/or HER2 activity.

The endo- and exo-1,7,7-Trimethylbicyclo-heptan-2-amines (Bornan-2-amines) and Their Acetamides

Carman, Raymond M.,Greenfield, Kay L.

, p. 1785 - 1790 (2007/10/02)

Melting points provide a poor method for differentiation between the exo and endo N-(bornan-2-yl)-acetamides, and have led to errors by previous workers.Spectral differences leading to unambiguous assignment are discussed in this paper.Trapping of the bornan-2-yl carbenium ion with acetonitrile leads to exo products.

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