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38489-85-9

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38489-85-9 Usage

Description

(4E)-4-[1-(hydroxyamino)ethylidene]-2-methoxycyclohexa-2,5-dien-1-one is a cyclic ketone with a hydroxyamino group and a methoxy group attached to a cyclohexadiene ring. It has a molecular structure of C11H13NO3 and a molecular weight of 207.23 g/mol. This unique structure and functional groups may provide potential applications in various fields.

Uses

Used in Pharmaceutical Industry:
(4E)-4-[1-(hydroxyamino)ethylidene]-2-methoxycyclohexa-2,5-dien-1-one is used as a pharmaceutical compound for its potential therapeutic properties. Its unique structure and functional groups may contribute to the development of new drugs and treatments.
Used in Organic Synthesis:
(4E)-4-[1-(hydroxyamino)ethylidene]-2-methoxycyclohexa-2,5-dien-1-one is used as an intermediate in organic synthesis for the production of various chemical compounds. Its functional groups can be utilized in the synthesis of other complex molecules.
Used in Material Science:
(4E)-4-[1-(hydroxyamino)ethylidene]-2-methoxycyclohexa-2,5-dien-1-one is used in material science for the development of new materials with unique properties. Its structure and functional groups may contribute to the creation of innovative materials with potential applications in various industries.
However, it is important to note that further research and analysis are needed to fully understand the properties and potential uses of (4E)-4-[1-(hydroxyamino)ethylidene]-2-methoxycyclohexa-2,5-dien-1-one.

Check Digit Verification of cas no

The CAS Registry Mumber 38489-85-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,8 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 38489-85:
(7*3)+(6*8)+(5*4)+(4*8)+(3*9)+(2*8)+(1*5)=169
169 % 10 = 9
So 38489-85-9 is a valid CAS Registry Number.

38489-85-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4E)-4-[1-(hydroxyamino)ethylidene]-2-methoxycyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names 1-(4-Hydroxy-3-methoxy-phenyl)-aethanon-oxim

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:38489-85-9 SDS

38489-85-9Relevant articles and documents

APPLICATIONS OF N6-SUBSTITUTED ADENOSINE DERIVATIVE AND N6-SUBSTITUTED ADENINE DERIVATIVE TO CALMING, HYPNOSES, CONVULSION RESISTANCE, EPILEPTIC RESISTANCE, PARKINSON DISEASE RESISTANCE, AND DEMENTIA PREVENTION AND TREATMENT

-

Paragraph 0142, (2018/10/27)

PROBLEM TO BE SOLVED: To prepare analgesics, hypnotic agents, anticonvulsant agents, antiepileptics, antiparkinson drugs, dementia prophylactics, and health care food. SOLUTION: The present invention relates to an N6-substituted adenosine derivative and an N6-substituted adenine derivative selected from the group consisting of specific compounds. The present invention also relates to a pharmaceutical composition at least comprising a therapeutically effective amount of the compounds and a pharmaceutically acceptable carrier. The invention further relates to the compounds used in preparation of analgesics, hypnotic agents, anticonvulsant agents, antiepileptics, antiparkinson drugs, dementia prophylactics, and health care food. COPYRIGHT: (C)2016,JPO&INPIT

The SAR analysis of TRPV1 agonists with the α-methylated B-region

Cho, Yongsung,Kim, Myeong Seop,Kim, Ho Shin,Ann, Jihyae,Lee, Jeewoo,Lee, Jiyoun,Pearce, Larry V.,Pavlyukovets, Vladimir A.,Morgan, Matthew A.,Blumberg, Peter M.

scheme or table, p. 5227 - 5231 (2012/09/07)

A series of TRPV1 agonists with amide, reverse amide, and thiourea groups in the B-region and their corresponding α-methylated analogues were investigated. Whereas the α-methylation of the amide B-region enhanced the binding affinities and potencies as agonists, that of the reverse amide and thiourea led to a reduction in receptor affinity. The analysis indicated that proper hydrogen bonding as well as steric effects in the B-region are critical for receptor binding.

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