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3,7,7-trimethylbicyclo[4.1.0]hept-3-ene-2,5-dione is a complex organic compound with the molecular formula C10H14O2. It is a bicyclic molecule, which means it consists of two carbon rings fused together. The compound features a 3-ene-2,5-dione functional group, indicating the presence of a carbonyl group at the 2nd and 5th positions, and a double bond at the 3rd position. Additionally, it has three methyl groups attached to the carbon atoms at positions 3, 7, and 7, which contribute to its unique structure and properties. 3,7,7-trimethylbicyclo[4.1.0]hept-3-ene-2,5-dione is known for its potential applications in the synthesis of various pharmaceuticals and other organic compounds due to its reactive functional groups and structural features.

6617-34-1

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6617-34-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6617-34-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,1 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6617-34:
(6*6)+(5*6)+(4*1)+(3*7)+(2*3)+(1*4)=101
101 % 10 = 1
So 6617-34-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O2/c1-5-4-6(11)7-8(9(5)12)10(7,2)3/h4,7-8H,1-3H3

6617-34-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,7,7-trimethylbicyclo[4.1.0]hept-3-ene-2,5-dione

1.2 Other means of identification

Product number -
Other names 3-carene-2,5-dione

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:6617-34-1 SDS

6617-34-1Upstream product

6617-34-1Relevant academic research and scientific papers

Comparative autoxidation of 3-Carene and α-Pinene: Factors governing regioselective hydrogen abstraction reactions

Rothenberg, Gadi,Yatziv, Yael,Sasson, Yoel

, p. 593 - 598 (2007/10/03)

Autoxidation reactions of 3-Carene 1 and α-Pinene 2 were performed using various homogeneous catalysts. Different product and regio- selectivities were observed. The factors that promote hydrogen abstraction (HA) reactions in both molecules are discussed, and it is proposed that the difference in the product selectivities is due to the lack of 'cyclic activation' in 2. Oxidation of 1 produced mainly 3-carene-5-one 3, while 2 yielded 2,3-epoxypinane 6 as the major product.

PRODUCTS OF THE CATALYTIC LIQUID-PHASE OXIDATION OF 3-CARENE

Vyglazov, O. G.,Manukov, E. N.,Fedorishcheva, M. N.,Ariko, N. G.,Chuiko, V. A.,Bazhina, G. N.

, p. 283 - 287 (2007/10/02)

The liquid-phase oxidation of 3-carene in the presence of various catalytic systems has been studied.The possibility has been shown of the directed preparation of 3-carene oxide, of ketones with a carane skeleton and a 7-membered ring, or of aromatic tertiary alcohols.

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