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828242-83-7

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828242-83-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 828242-83-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,8,2,4 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 828242-83:
(8*8)+(7*2)+(6*8)+(5*2)+(4*4)+(3*2)+(2*8)+(1*3)=177
177 % 10 = 7
So 828242-83-7 is a valid CAS Registry Number.

828242-83-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[2-[tert-butyl(dimethyl)silyl]oxyethoxy]benzaldehyde

1.2 Other means of identification

Product number -
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

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:828242-83-7 SDS

828242-83-7Relevant articles and documents

Anti-inflammatory agents

-

Page/Page column 149, (2016/02/05)

Disclosed are novel compounds that are useful in regulating the expression of interleukin-6 (IL-6) and/or vascular cell adhesion molecule-1 (VCAM-1), and their use in the treatment and/or prevention of cardiovascular and inflammatory diseases and related disease states, such as, for example, atherosclerosis, asthma, arthritis, cancer, multiple sclerosis, psoriasis, and inflammatory bowel diseases, and autoimmune disease(s). Also, disclosed are compositions comprising the novel compounds, as well as methods for their preparation.

Photoactivatable fluorescein derivatives caged with a (3-hydroxy-2- naphthalenyl)methyl group

Nekongo, Emmanuel E.,Popik, Vladimir V.

, p. 7665 - 7671 (2014/09/17)

The (3-hydroxy-2-naphthalenyl)methyl (NQMP) group represents an efficient photocage for fluorescein-based dyes. Thus, irradiation of the 6-NQMP ether of 2'-hydroxymethylfluorescein with low-intensity UVA light results in a 4-fold increase in emission inte

ARYLAMINE-SUBSTITUTED QUINAZOLINONE COMPOUNDS

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Page 70, (2010/02/10)

Compounds represented by Formula (I) which are useful as are alpha-1A/B adrenoceptor antagonists, to methods of treating conditions associated with the activity of alpha-1A/B adrenoceptors, and to methods of making said compounds, wherein Ar, Z, R, R', R

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