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90878-20-9

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90878-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90878-20-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,8,7 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 90878-20:
(7*9)+(6*0)+(5*8)+(4*7)+(3*8)+(2*2)+(1*0)=159
159 % 10 = 9
So 90878-20-9 is a valid CAS Registry Number.

90878-20-9SDS

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 2-amino-benzaldehyde-(O-methyl oxime )

1.2 Other means of identification

Product number -
Other names (E)-O-methyloxime-2-aminobenzaldehyde

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:90878-20-9 SDS

90878-20-9Downstream Products

90878-20-9Relevant articles and documents

Imidazoline derivatives as alpha-1A adrenoceptor ligands

-

Page/Page column 26, (2010/02/11)

Compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof are disclosed. Such compounds are useful in the treatment of Alpha-1A mediated diseases or conditions such as urinary incontinence.

Derivatives of Phenylurea as Antagonists of Mice, Rat, Guinea Pig, and Rabbit 5-HT3 Receptors

Hansen, John Bondo,Christensen, Birgitte,Weiss, Jan,Suzdak, Peter D.,Sheardown, Malcolm J.,et al.

, p. 308 - 315 (2007/10/03)

1,2,4-Oxadiazolyl- and O-alkyloximinomethyl-substituted phenylureas equipotently bind to 5-HT3 receptors from different species in vitro in contrast to the normal 10-100 fold lower affinity for guinea pig ileal receptors. Compared to the in vitro receptor

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