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556826-36-9

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556826-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 556826-36-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,6,8,2 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 556826-36:
(8*5)+(7*5)+(6*6)+(5*8)+(4*2)+(3*6)+(2*3)+(1*6)=189
189 % 10 = 9
So 556826-36-9 is a valid CAS Registry Number.

556826-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-methylazulen-4-yl)propanoic acid

1.2 Other means of identification

Product number -
Other names 4-Azulenepropanoic acid,2-methyl

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:556826-36-9 SDS

556826-36-9Upstream product

556826-36-9Downstream Products

556826-36-9Relevant articles and documents

A practical approach for the preparation of monofunctional azulenyl squaraine dye

Pham, Wellington,Weissleder, Ralph,Tung, Ching-Hsuan

, p. 3975 - 3978 (2007/10/03)

The synthesis of monofunctional azulenyl squaraine dye NIRQ700 is described. The essential azulene intermediate 3, 1-(methoxycarbonyl)-2-methylazulene, was achieved via [8+2] cycloaddition between lactone 2, 2H-3-methoxycarbonyl-cyclohepta[b]furan-2-one, and the in situ generated vinyl ethers under high temperature and pressure conditions. Methylation on the cycloheptatriene ring of 2-methyl azulene 6 via Meisenheimer-type intermediate following Schrott's method formed the carboxylic acid intermediate 9, 3-(2-methyl-azulen-4-yl)-propionic acid. Condensation of 9 with squaric acid provided the title compound NIRQ700 at moderate yields. The non-fluorescent squaraine dye NIRQ700 absorbed in a 600-700 nm range and potentially can be used to quench a number of available NIR fluorochromes in order to extend the spectrum of biological quenching assays.

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