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134823-10-2

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134823-10-2 Usage

Chemical structure

A complex structure that includes a chromene ring, a fluorophenoxy group, a methylurea moiety, and a hydroxyl group.

Potential pharmaceutical applications

Due to its structural features, it could potentially interact with biological targets in the body.

Hydrophobicity

The presence of the fluorophenoxy group suggests that it may have some degree of hydrophobicity.

Hydrogen bonding capabilities

The hydroxyl and methylurea groups indicate potential hydrogen bonding capabilities.

Further research needed

Further research and evaluation would be needed to fully understand the properties and potential uses of this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 134823-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,8,2 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 134823-10:
(8*1)+(7*3)+(6*4)+(5*8)+(4*2)+(3*3)+(2*1)+(1*0)=112
112 % 10 = 2
So 134823-10-2 is a valid CAS Registry Number.

134823-10-2SDS

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 1-[[6-(4-fluorophenoxy)-2H-chromen-3-yl]methyl]-1-hydroxy-3-methylurea

1.2 Other means of identification

Product number -
Other names 1-{[6-(4-fluorophenoxy)-2h-chromen-3-yl]methyl}-1-hydroxy-3-methylurea

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:134823-10-2 SDS

134823-10-2Upstream product

134823-10-2Downstream Products

134823-10-2Relevant articles and documents

Substituted chromenes as potent, orally active 5-lipoxygenase inhibitors

Satoh,Stanton,Hutchison,Libby,Kowalski,Lee,White,Kimble

, p. 3580 - 3594 (2007/10/02)

A series of chromene derivatives was synthesized and evaluated for their in vitro and ex vivo 5-lipoxygenase (5-LO) inhibitory activity. These compounds were prepared by condensation of appropriate salicyl aldehydes with α,β-unsaturated carbonyl compounds

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