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1,2,4-Methenopentalene, 1,2,3,3a,4,6a-hexahydro-, also known as 1,2,4-Metheno-1,2,3,3a,4,6a-hexahydropentalene, is a chemical compound with the molecular formula C6H8. It is a cyclic hydrocarbon with a unique structure, featuring a metheno bridge (a carbon-carbon double bond) and a hexahydro (six hydrogen atoms) framework. 1,2,4-Methenopentalene, 1,2,3,3a,4,6a-hexahydro- is an example of a polycyclic aromatic hydrocarbon (PAH) and is known for its potential applications in organic synthesis and as a precursor in the production of various chemical compounds. Due to its complex structure and reactivity, it is typically studied and used in specialized chemical research and industrial processes.

7785-10-6

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7785-10-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7785-10-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,8 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7785-10:
(6*7)+(5*7)+(4*8)+(3*5)+(2*1)+(1*0)=126
126 % 10 = 6
So 7785-10-6 is a valid CAS Registry Number.

7785-10-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name tetracyclo[4.2.0.02,4.03,7]nonene-8

1.2 Other means of identification

Product number -
Other names deltacyclene

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:7785-10-6 SDS

7785-10-6Relevant academic research and scientific papers

5-TETRACYCLO2,4.03,6>OCT-7-ENYL CARBENE; AN ATTEMPTED SYNTHESIS OF A FENESTRANE DERIVATE.

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

, p. 3051 - 3058 (2007/10/02)

The title carbene was generated at low temperature with the objectiv to effect intramolecular cyclopropanation of its double bond.Labelling studies showed intramolecular C-C bond insertation followed by intramolecular reverse Diels Alder reaction to be the major pathway to the products.

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