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769-31-3

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769-31-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 769-31-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 769-31:
(5*7)+(4*6)+(3*9)+(2*3)+(1*1)=93
93 % 10 = 3
So 769-31-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H10/c1-9-7-8-10-5-3-2-4-6-11(9)10/h2-8H,1H3

769-31-3SDS

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 1-methylazulene

1.2 Other means of identification

Product number -
Other names 3-Methylazulene

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:769-31-3 SDS

769-31-3Upstream product

769-31-3Relevant articles and documents

Azulenylcarbene and Naphthylcarbene Isomerizations. Falling Solid Flash Vacuum Pyrolysis

Kvaskoff, David,Becker, Jürgen,Wentrup, Curt

, p. 5030 - 5034 (2015/05/27)

1-Azulenylcarbene 18 has been generated from 5-(1-azulenyl)tetrazole and the sodium salt of azulene-1-carbaldehyde tosylhydrazone using the falling solid flash vacuum pyrolysis (FS-FVP) method. The principal products, which are also formed from both 1- and 2-naphthylcarbenes, cyclobuta[de]naphthalene 6, cyclopenta[cd]indene 16, and benzofulvenallene 17, are explained in terms of two reaction paths, (a) a rearrangement to benzofulvenyl-7-carbene 13 and (b) a rearrangement to 1-naphthylcarbene 1. Moreover, 16 is also formed from 2-azulenylcarbene 30, thereby indicating the occurrence of a 2-azulenylcarbene-1-azulenylcarbene rearrangement. The reaction mechanisms are supported by density functional theory calculations at the B3LYP/6-31G?? level, which indicate that all the rearrangements have activation barriers of 35 kcal/mol, thus making them readily achievable under FVP conditions. Chemical Presented.

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