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160194-39-8

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160194-39-8 Usage

Uses

5-(1H-1,2,4-Triazol-1-ylmethyl)-1H-indole-3-ethanol is an intermediate in the synthesis of Rizatriptan Benzoate (R545000); a selective serotonin 5-HT1D receptor agonist and a potential anti-migraine drug.

Check Digit Verification of cas no

The CAS Registry Mumber 160194-39-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,1,9 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 160194-39:
(8*1)+(7*6)+(6*0)+(5*1)+(4*9)+(3*4)+(2*3)+(1*9)=118
118 % 10 = 8
So 160194-39-8 is a valid CAS Registry Number.

160194-39-8SDS

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 2-[5-(1,2,4-triazol-1-ylmethyl)-1H-indol-3-yl]ethanol

1.2 Other means of identification

Product number -
Other names Rizatriptan benzoate impurity F [EP]

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:160194-39-8 SDS

160194-39-8Relevant articles and documents

COMPOSITIONS AND METHODS FOR TREATING OPHTHALMIC DISEASES

-

Page/Page column 28, (2008/06/13)

This invention relates to CXCR4 inhibitors and their use in treating and/or preventing a variety of angiogenic, microvascular and ocular disorders including primary indications for diabetic retinopathy, macular degeneration (such as wet or neovascular age

Azetidine, pyrrolidine and piperidine derivatives

-

, (2008/06/13)

A class of substituted azetidine, pyrrolidine and piperidine derivatives are selective agonists of 5-HT1 -like receptors, being potent agonists of the human 5-HT1Dα receptor subtype whilst possessing at least a 10-fold selective affinity for the 5-HT1Dα receptor subtype relative to the 5-HT1Dβ subtype; they are therefore useful in the treatment and/or prevention of clinical conditions, in particular migraine and associated disorders, for which a subtype-selective agonist of 5-HT1D receptors is indicated, whilst eliciting fewer side-effects, notably adverse cardiovascular events, than those associated with non-subtype-selective 5-HT1D receptor agonists.

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