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2-Propenenitrile, 3-[(4-bromophenyl)sulfonyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14223-30-4

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14223-30-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14223-30-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,2 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14223-30:
(7*1)+(6*4)+(5*2)+(4*2)+(3*3)+(2*3)+(1*0)=64
64 % 10 = 4
So 14223-30-4 is a valid CAS Registry Number.

14223-30-4SDS

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 3-(4-bromophenyl)sulfonylprop-2-enenitrile

1.2 Other means of identification

Product number -
Other names -

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:14223-30-4 SDS

14223-30-4Relevant academic research and scientific papers

Non-basic ligands for aminergic GPCRs: The discovery and development diaryl sulfones as selective, orally bioavailable 5-HT2A receptor antagonists for the treatment of sleep disorders

Ladduwahetty, Tammy,Gilligan, Myra,Humphries, Alexander,Merchant, Kevin J.,Fish, Rebecca,McAlister, George,Ivarsson, Magnus,Dominguez, Maria,O'Connor, Desmond,MacLeod, Angus M.

scheme or table, p. 3708 - 3712 (2010/09/18)

Scaffold hopping from a non-basic series of 5-HT2A receptor antagonists developed in-house that possessed reduced activity in vivo enabled the discovery of a novel series of diaryl sulfones that gave excellent occupancy on oral dosing. Not only does this work further demonstrate that oral bioavailability of a given series can be enhanced by improving physicochemical parameters such as log P, but it corroborates the growing evidence that a protonated amine is not essential for affinity at aminergic GPCRs.

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