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(4aS,8aα)-Decahydro-1,1,4aβ-trimethyl-6-methylene-5β-(3-methyl-3-pentenyl)naphthalene is a complex organic compound with a molecular formula of C20H32. It is a derivative of naphthalene, a bicyclic aromatic hydrocarbon, and features a decahydro (10-carbon) saturated ring structure. The compound has three methyl groups attached to the naphthalene core, with one at the 1-position, another at the 4a-position, and a third at the 3-methyl-3-pentenyl group. The 6-methylene group indicates the presence of a double bond between carbons 6 and 7, and the 5β-(3-methyl-3-pentenyl) group signifies an isoprene unit attached to the 5-position of the naphthalene ring. This chemical is characterized by its unique stereochemistry, with the 4aS and 8aα configurations indicating the specific spatial arrangement of the atoms within the molecule.

6138-92-7

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6138-92-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6138-92-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,3 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6138-92:
(6*6)+(5*1)+(4*3)+(3*8)+(2*9)+(1*2)=97
97 % 10 = 7
So 6138-92-7 is a valid CAS Registry Number.
InChI:InChI=1/C21H17ClN2O/c22-17-12-10-16(11-13-17)20-23-19-9-5-4-8-18(19)21(25)24(20)14-15-6-2-1-3-7-15/h1-13,20,23H,14H2

6138-92-7SDS

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-benzyl-2-(4-chlorophenyl)-1,2-dihydroquinazolin-4-one

1.2 Other means of identification

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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

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More Details:6138-92-7 SDS

6138-92-7Downstream Products

6138-92-7Relevant academic research and scientific papers

Amber-type odorants from communic acids

Barrero, Alejandro F.,Altarejos, Joaquin,Alvarez-Manzaneda, Enrique J.,Ramos, Jose M.,Salido, Sofia

, p. 9525 - 9534 (1993)

A mixture of the methyl esters of communic acids (3b, 4b, 5b) was used in the synthesis of the ambergris-type odorants Ambrox (1) and ambracetal (2). Both syntheses involve methyl ketone 7 as the key intermediate.

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