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80139-82-8

80139-82-8

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80139-82-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80139-82-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,1,3 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 80139-82:
(7*8)+(6*0)+(5*1)+(4*3)+(3*9)+(2*8)+(1*2)=118
118 % 10 = 8
So 80139-82-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H19ClN2O/c1-17(2)13(18)14(7-9-16-10-8-14)11-3-5-12(15)6-4-11/h3-6,16H,7-10H2,1-2H3

80139-82-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-chlorophenyl)-N,N-dimethylpiperidine-4-carboxamide

1.2 Other means of identification

Product number -
Other names 4-Piperidinecarboxamide,4-(4-chlorophenyl)-N,N-dimethyl

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:80139-82-8 SDS

80139-82-8Downstream Products

80139-82-8Relevant articles and documents

Phenylpiperidine-benzoxazinones as urotensin-II receptor antagonists: Synthesis, SAR, and in vivo assessment

Luci, Diane K.,Ghosh, Shyamali,Smith, Charles E.,Qi, Jenson,Wang, Yuanping,Haertlein, Barbara,Parry, Tom J.,Li, Jian,Almond Jr., Harold R.,Minor, Lisa K.,Damiano, Bruce P.,Kinney, William A.,Maryanoff, Bruce E.,Lawson, Edward C.

, p. 6489 - 6492 (2008/03/13)

Various 4-phenylpiperidine-benzoxazin-3-ones were synthesized and biologically evaluated as urotensin-II (U-II) receptor antagonists. Compound 12i was identified from in vitro evaluation as a low nanomolar antagonist against both rat and human U-II receptors. This compound showed in vivo efficacy in reversing the ear-flush response induced by U-II in rats.

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