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170729-79-0

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  • {2R-[2α(S),3α]}-2-{1-[3,5-Bis-(trifluoromethyl)-phenyl]-ethoxy}-3-(4-fluorophenyl)-morpholine

    Cas No: 170729-79-0

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  • best quality /favorable price 170729-79-0 good supplier / [2R-[2aR*),3a]-2-[1-[3,5-Bis(trifluoromethyl)phenyl]ethoxy]-3-(4-fluorophenyl)morpholine

    Cas No: 170729-79-0

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170729-79-0 Usage

Chemical Properties

Yellow Oil

Uses

Different sources of media describe the Uses of 170729-79-0 differently. You can refer to the following data:
1. A metabolite of Aprepitant.
2. A metabolite of Aprepitant

Check Digit Verification of cas no

The CAS Registry Mumber 170729-79-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,7,2 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 170729-79:
(8*1)+(7*7)+(6*0)+(5*7)+(4*2)+(3*9)+(2*7)+(1*9)=150
150 % 10 = 0
So 170729-79-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H18F7NO2/c1-11(13-8-14(19(22,23)24)10-15(9-13)20(25,26)27)30-18-17(28-6-7-29-18)12-2-4-16(21)5-3-12/h2-5,8-11,17-18,28H,6-7H2,1H3/t11-,17-,18+/m0/s1

170729-79-0SDS

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 2-(R)-[1-(S)-(3,5-Bis(trifluoromethyl)phenyl)ethoxy]-3-(S)-fluorophenylmorpholine

1.2 Other means of identification

Product number -
Other names [2R-[2aR*),3a]-2-[1-[3,5-Bis(trifluoromethyl)phenyl]ethoxy]-3-(4-fluorophenyl)morpholine

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:170729-79-0 SDS

170729-79-0Upstream product

170729-79-0Downstream Products

170729-79-0Relevant articles and documents

Synthesis of all enantiomerically pure diastereomers of aprepitant

Gangula, Srinivas,Elati, Chandrashekhar R.,Mudunuru, Satish Varma,Nardela, Anitha,Dongamanti, Ashok,Bhattacharya, Apurba,Bandichhor, Rakeshwar

experimental part, p. 2254 - 2268 (2010/09/11)

Syntheses of all eight enantiomerically pure diastereomers of aprepitant and assignment of absolute configuration at newly generated stereocenters by NMR and X-ray crystallographic analysis were achieved. Copyrigh

MORPHOLINE AND THIOMORPHOLINE TACHYKININ RECEPTOR ANTAGONISTS

-

, (2008/06/13)

Substituted heterocycles of the general structural formula: STR1 are tachykinin receptor antagonists useful in the treatment of inflammatory diseases, pain or migraine, asthma and emesis, and calcium channel blockers useful in the treatment of cardiovascular conditions such as angina, hypertension or ischemia.

MORPHOLINE COMPOUNDS ARE PRODRUGS USEFUL AS TACHYKININ RECEPTOR ANTAGONISTS

-

, (2008/06/13)

Substituted heterocycles of the general structural formula: STR1 are tachykinin receptor antagonists useful in the treatment of inflammatory diseases, pain or migraine, asthma, and emesis.

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