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(3-CHLORO-4-METHOXY-PHENYL)-HYDRAZINE, also known as a substituted phenyl hydrazine, is a chemical compound with a distinctive phenyl-hydrazine structure. This variant is characterized by the presence of a chlorine atom (3-chloro) and a methoxy group (4-methoxy) on the phenyl ring. Its properties and potential uses are derived from this structure, and it can be utilized in various synthetic chemistry procedures.

24630-85-1

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24630-85-1 Usage

Uses

Used in Pharmaceutical Industry:
(3-CHLORO-4-METHOXY-PHENYL)-HYDRAZINE is used as an intermediate compound for the synthesis of various pharmaceuticals. Its unique structure allows for the creation of a wide range of products with different therapeutic applications.
Used in Chemical Industry:
(3-CHLORO-4-METHOXY-PHENYL)-HYDRAZINE is used as a building block in the production of dyes and other returned substances. Its reactivity and structural features make it a valuable component in the synthesis of these compounds.
Used in Pesticide Industry:
(3-CHLORO-4-METHOXY-PHENYL)-HYDRAZINE is used as a precursor in the development of certain pesticides. Its chemical properties contribute to the effectiveness of these agricultural chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 24630-85-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,3 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 24630-85:
(7*2)+(6*4)+(5*6)+(4*3)+(3*0)+(2*8)+(1*5)=101
101 % 10 = 1
So 24630-85-1 is a valid CAS Registry Number.

24630-85-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-Chloro-4-methoxyphenyl)hydrazine

1.2 Other means of identification

Product number -
Other names 3-Chloro-4-methoxy-phenylhydrazin

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:24630-85-1 SDS

24630-85-1Relevant academic research and scientific papers

Aminopyridinecarboxamide-based inhaled IKK-2 inhibitors for asthma and COPD: Structure-activity relationship

Xie, Jin,Poda, Gennadiy I.,Hu, Yiding,Chen, Natalie X.,Heier, Richard F.,Wolfson, Serge G.,Reding, Matthew T.,Lennon, Patrick J.,Kurumbail, Ravi G.,Selness, Shaun R.,Li, Xiong,Kishore, Nandini N.,Sommers, Cynthia D.,Christine, Lori,Bonar, Sheri L.,Venkatraman, Neetu,Mathialagan, Sumathy,Brustkern, Sarah J.,Huang, Horng-Chih

experimental part, p. 1242 - 1255 (2011/04/12)

Installation of sites for metabolism in the lead compound PHA-767408 was the key focus of the IKK-2 inhaled program. This paper reports our efforts to identify a novel series of aminopyridinecarboxamide-based IKK-2 inhibitors, which display low nanomolar potency against IKK-2 with long duration of action (DOA), and metabolically labile to phase I and/or phase II metabolizing enzymes with potential capability for multiple routes of clearance. Several compounds have demonstrated their potential usefulness in the treatment of asthma and chronic obstructive pulmonary disease (COPD).

Synthesis of COX-2 and FAAH inhibitors

-

, (2008/06/13)

Methods for preparing indoles that are useful COX-2 inhibitors and intermediates useful in such methods are described.

Pyridazino quinoline compounds

-

, (2008/06/13)

The invention relates to pyridazinoquinoline compounds of the formulas B and B′ wherein Ring A is selected from an ortho fused aromatic or heteroaromatic five- or six-membered ring and R1, R3and R4are substituents selected from halo, OH, OCF3, NO2, CN, NR′R″, SO2NR′R″, SOmR′alkyl, and a variety of alkyl, aryl, heterocyclic and heteroaryl groups, to pharmaceutical compositions containing them and to methods utilizing them for the treatment of neurological disorders.

Pyridazion quinoline compounds

-

, (2008/06/13)

The present invention relates to compounds, pharmaceutical compositions and methods of using compounds of formula (I) in the treatment and/or prevention of certain diseases or conditions. In formula (I), A is chosen from ortho substituted aryl or heteroaryl species, X is chosen from --OH, --SH, NHR and R 1 or R 2 is chosen from --(CH 2) n L wherein L may be selected from a variety of substituents including aryl, heteroaryl and heterocyclic groups. The compounds are useful in treating and/or preventing neurological disorders associated with excitatory amino acids. STR1

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