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6703-30-6

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6703-30-6 Usage

General Description

(1R,2R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptane-2-carboxylic acid, also known as bornane carboxylic acid, is a bicyclic organic compound with a carboxylic acid group attached to a bicyclo[2.2.1]heptane ring system. It is a colorless, solid compound with a strong odor. It is commonly used as a chiral building block in the pharmaceutical industry for the synthesis of various drugs and other biologically active compounds. Due to its rigid and chiral structure, it is often used as a starting material for the preparation of chiral catalysts and ligands in asymmetric synthesis. Additionally, its unique structure and properties make it a valuable compound for research and development in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 6703-30-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,0 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6703-30:
(6*6)+(5*7)+(4*0)+(3*3)+(2*3)+(1*0)=86
86 % 10 = 6
So 6703-30-6 is a valid CAS Registry Number.

6703-30-6SDS

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 endo-1,7,7-Trimethylnorbornane-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names (+-)-1.7.7-Trimethyl-norbornan-carbonsaeure-(2endo)

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:6703-30-6 SDS

6703-30-6Downstream Products

6703-30-6Relevant articles and documents

Rearrangement approaches to cyclic skeletons. IX. Stereoselective total synthesis of (±)-camphorenone based on a ring-contraction of bicyclo[3.2.1]oct-6-en-2-one. Reliable one-step diazo transfer followed by a Wolff rearrangement

Uyehara,Takehara,Ueno,Sato

, p. 2687 - 2694 (2007/10/03)

A direct diazo transfer reaction to bicyclo[3.2.1]oct-6-en-2-ones and related compounds was accomplished by treatments with 2,4,6-triisopropylbenzenesulfonyl azide and potassium t-butoxide at -78°C in THF. A Wolff rearrangement of the resulting α-diazoketones in the presence of water gave ring-contraction products, bicyclo[2.2.1]heptenecarboxylic acids. Using these two transformations the total synthesis of (±)-camphorenone was achieved stereoselectively, starting from 1-methoxybicyclo[2.2.2]oct-5-en-2-one.

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