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Apocamphane is a bicyclic monoterpene, a class of organic compounds derived from isoprene units, characterized by its unique structure consisting of two fused rings. It is found in various essential oils, particularly in the plant family Lamiaceae, and is known for its pleasant, earthy aroma. Apocamphane has potential applications in the fragrance and flavor industries due to its scent, and it may also have biological activities, although further research is needed to fully understand its properties and potential uses.

2034-53-9

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2034-53-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2034-53-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,3 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2034-53:
(6*2)+(5*0)+(4*3)+(3*4)+(2*5)+(1*3)=49
49 % 10 = 9
So 2034-53-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H16/c1-9(2)7-3-4-8(9)6-5-7/h7-8H,3-6H2,1-2H3

2034-53-9SDS

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 7,7-Dimethyl-bicyclo(2.2.1)heptane

1.2 Other means of identification

Product number -
Other names -

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:2034-53-9 SDS

2034-53-9Downstream Products

2034-53-9Relevant academic research and scientific papers

Oxidative coupling of 7,7-dilithionorbornane; 7,7′-dilithio-7,7′-dinorbornyl, a new vic-dilithioalkane prone to a new mode of decomposition

Vlaar, Cornelis P.,Klumpp, Gerhard W.

, p. 4651 - 4654 (2007/10/02)

7,7-Dilithionorbornane reacts with butyl halides at -100°C to give 7,7′-dilithio-7,7′-dinorbornyl (30%), which is easily oxidized to 7,7′-dinorbornylidene.

Preparation and Some Properties of 7,7-Dilithionorbornane

Vlaar, Cornelis P.,Klumpp, Gerhard W.

, p. 2951 - 2952 (2007/10/02)

7,7-Dilithionorbornane 4a is formed from 7,7-dibromonorbornane 4b by reduction with 4.5 equiv of lithium p,p'-di-tert-butylbiphenyl at -100 deg C, at which temperature it adds to ethylene.On warming it rearranges to 1-lithio-5-(2-lithioethyl)cyclopentene 5.

MECHANISM OF THE THERMAL CONVERSION OF TETRACYCLO(3.3.0.02,4.03.6)OCT-7-ENE INTO DIHYDROPENTALENES

Stapersma, J.,Rood, I. D. C.,Klumpp, G. W.

, p. 2201 - 2212 (2007/10/02)

One of a number of possible mechanisms has been established for the title reaction.

SYNTHESIS OF TETRACYCLO2,4.03,6>OCT-7-ENE AND SOME OF ITS DERIVATIVES

Stapersma, J.,Rood, I. D. C.,Klumpp, G. W.

, p. 191 - 199 (2007/10/02)

A full account is given of the synthesis of the title compound, its 7,8-dihydro-analogue and of some of its derivatives.

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