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Tricyclic[3.2.1.0~2,4~]octan-8-ol, also known as bicyclo[3.2.1]octanol, is a cyclic alcohol with a unique tricyclic structure. It consists of three fused rings, with the central ring being a cyclopropane ring, and the other two being cyclohexane rings. The molecule has a hydroxyl group (-OH) attached to the eighth carbon atom, which is crucial for its chemical properties and reactivity. tricyclo[3.2.1.0~2,4~]octan-8-ol is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its complex structure and functional group make it an interesting target for organic chemists and researchers in the field of drug development.

7076-81-5

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7076-81-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7076-81-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,7 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7076-81:
(6*7)+(5*0)+(4*7)+(3*6)+(2*8)+(1*1)=105
105 % 10 = 5
So 7076-81-5 is a valid CAS Registry Number.

7076-81-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Tricyclo[3.2.1.0<sup>2,4</sup>]octan-8-ol

1.2 Other means of identification

Product number -
Other names endo-norbornane oxide

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:7076-81-5 SDS

7076-81-5Downstream Products

7076-81-5Relevant academic research and scientific papers

Probing the nature and extent of stabilization within foiled carbenes: Homoallylic participation by a neighboring cyclopropane ring

Apeland, Ingrid Malene,K?hlig, Hanspeter,Lorbeer, Eberhard,Brinker, Udo H.

, p. 4879 - 4885 (2013/07/11)

Oxadiazoline 6 was synthesized to generate endo-tricyclo[3.2.1.0 2,4]octan-8-ylidene (3) by either photolysis or thermolysis. Diastereomer 6a thermally decomposed twice as fast as 6b. Carbene 3 was trapped stereoselectively by acrylonitrile and diethylamine in high yields. It behaved as a nucleophilic carbene with electron-poor alkenes, like acrylonitrile, but as an electrophile with very electron-rich species, such as diethylamine. However, when the reactions were performed in cyclohexane and cyclohexene, isomerization of 3 was favored. Replacement of the double bond in 7-norbornenylidene (1) by the single bond in the endo-fused cyclopropane unit of carbene 3 led to similar outcomes. Carbene 3 rightfully belongs to the family of foiled carbenes.

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