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85689-01-6

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85689-01-6 Usage

Classification

Bicyclic organic compound

Structure

Contains a seven-membered ring system with a hydroxy group attached to one of the carbon atoms

Use

Commonly used in the fragrance industry as a scent additive

Odor

Pleasant, floral-like

Applications

Found in perfumes and scented products to add a fresh and uplifting aroma

Medicinal properties

Studied for potential anti-inflammatory and anti-oxidant properties

Check Digit Verification of cas no

The CAS Registry Mumber 85689-01-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,6,8 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 85689-01:
(7*8)+(6*5)+(5*6)+(4*8)+(3*9)+(2*0)+(1*1)=176
176 % 10 = 6
So 85689-01-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H10NO/c8-7-4-5-1-2-6(7)3-5/h5-6H,1-4H2

85689-01-6SDS

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 3-λ<sup>1</sup>-oxidanyl-3-azabicyclo[2.2.1]heptane

1.2 Other means of identification

Product number -
Other names 2-Azabicyclo(2.2.1)heptane,2-hydroxy

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:85689-01-6 SDS

85689-01-6Relevant articles and documents

Nitrenium and Carbenium Ions in Rearrangements of 2-Azabicyclic Systems

Heesing, Albert,Herdering, Wilhelm

, p. 1081 - 1096 (2007/10/02)

An ionic mechanism proceeding in intimate ion pairs is suggested for the rearrangement of N-sulfonyloxy derivatives of 2-azabicycloheptane and -hept-5-ene (e. g. 9, 11 -> 10, 12). 1.Experiments with 18O labelled educts show partial scrambling dependend both on structure of educt and solvent. 2.In methanol the intermediate carbenium ions (19, 23) react to give methoxy compounds. 3.MINDO/3-calculations are in agreement with the experiments: a) In the saturated systems the nitrenium ion 20 is a stable intermediate. b) The optimized geometries of the rearranged carbenium ions (21, 23) are consistent with the products obtained in methanol.

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