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6-Bromo-2,2-dimethyl-2H-chromene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82305-04-2

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82305-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82305-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,3,0 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82305-04:
(7*8)+(6*2)+(5*3)+(4*0)+(3*5)+(2*0)+(1*4)=102
102 % 10 = 2
So 82305-04-2 is a valid CAS Registry Number.

82305-04-2SDS

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 6-bromo-2,2-dimethylchromene

1.2 Other means of identification

Product number -
Other names 2H-1-Benzopyran,6-bromo-2,2-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:82305-04-2 SDS

82305-04-2Relevant academic research and scientific papers

Relaxant Activity of 4-Amido-3,4-dihydro-2H-1-benzopyran-3-ols and 4-Amido-2H-1-benzopyrans on Guinea Pig Isolated Trachealis

Buckle, Derek R.,Arch, Jonathon R. S.,Fenwick, Ashley E.,Houge-Frydrych, Catherine S. V.,Pinto, Ivan L.,et al.

, p. 3028 - 3034 (2007/10/02)

A series of 4-amido-3,4-dihydro-2H-benzopyran-3-ols and 4-amido-2H-1-benzopyrans related to the potassium channel activator cromakalim have been prepared and evaluated for their relaxant activity in guinea pig isolated tracheal spirals.Several analogues show enhanced relaxant activity relative to cromakalim in this preparation and the rank order of potency for those substituents investigated at C-6 was CF3>CN>C2H5>aza>=CH3.One compound, trans-3,4-dihydro-2,2-dimethyl-4-(2-oxopiperidin-1-yl)-7-(trifluoromethyl)-2H-1-benzopyran-3-ol (24), was resolved into its two enantiomers and the activity was shown to reside essentially in the (+)-isomer, adding further support to the suggestion that the smooth muscle receptor for these potassium channel activators is stereoselective.

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