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40475-25-0

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40475-25-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40475-25-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,4,7 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40475-25:
(7*4)+(6*0)+(5*4)+(4*7)+(3*5)+(2*2)+(1*5)=100
100 % 10 = 0
So 40475-25-0 is a valid CAS Registry Number.
InChI:InChI=1/C21H27ClN2O4/c1-26-20-8-5-17(13-21(20)27-2)24-11-9-23(10-12-24)14-18(25)15-28-19-6-3-16(22)4-7-19/h3-8,13,18,25H,9-12,14-15H2,1-2H3

40475-25-0SDS

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 1-(4-chlorophenoxy)-3-[4-(3,4-dimethoxyphenyl)piperazin-1-yl]propan-2-ol

1.2 Other means of identification

Product number -
Other names 1-(4-chloro-phenoxy)-3-[4-(3,4-dimethoxy-phenyl)-piperazin-1-yl]-propan-2-ol

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:40475-25-0 SDS

40475-25-0Upstream product

40475-25-0Downstream Products

40475-25-0Relevant articles and documents

3-Tertiary amino-1-aryloxy- or aryl-propanes and -propan -2-ols and some related compounds

Gupta,Mukerji,Chatterjee,Rastogi,Anand,Dube,Sur Jr.,Mukerji,Srimal

, p. 241 - 246 (2007/10/04)

The synthesis and pharmacological activity of some 3 tertiary amino 1 aryloxy or 1 aryl, 1 thiophenoxy and 1 anilino propan 2 ols and propanes, particularly those derived from N phenylpiperazines are described. Effect of substituents (nature/position) on the phenyl ring, the phenoxy ring as well as alteration in the hydroxylic function vis a vis the structure activity relationships (SAR) are discussed. In general, the 1 aryloxy compounds have hypotensive activity this being more pronounced in those carrying an o substituent on the phenyl ring, while m and p substituted derivatives have their effect primarily on the CNS. Variations in the phenoxy moiety do not significantly alter the intrinsic activity. The 1 aryl compounds, on the other hand, have significant CNS activity, which is markedly affected by the substituents on the 1 aryl residue.

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