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2-Chloro-3-methoxybenzaldehyde is a chemical compound characterized by the molecular formula C8H7ClO2. It is a pale yellow solid that features a benzaldehyde group, a chlorine atom, and a methoxy group. 2-CHLORO-3-METHOXYBENZALDEHYDE is known for its strong and distinct odor and is classified as a hazardous material, necessitating careful handling and storage. It is widely utilized in organic synthesis as an intermediate for the production of pharmaceuticals, agricultural chemicals, and dyes, making it a versatile component in the creation of a broad spectrum of other organic compounds.

54881-49-1

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54881-49-1 Usage

Uses

Used in Pharmaceutical Industry:
2-Chloro-3-methoxybenzaldehyde is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs and medicinal compounds. Its unique structure allows for the creation of a wide range of organic compounds that can be tailored for specific therapeutic applications.
Used in Agricultural Chemicals Industry:
In the agricultural sector, 2-Chloro-3-methoxybenzaldehyde is employed as an intermediate in the production of agricultural chemicals. Its chemical properties make it suitable for the development of compounds that can be used in crop protection and other agricultural applications.
Used in Dyes Industry:
2-Chloro-3-methoxybenzaldehyde is utilized in the dyes industry as an intermediate for the synthesis of various dyes. Its chemical structure contributes to the creation of dyes with specific color properties and characteristics, making it a valuable component in the production of a diverse array of dyes.
Used in Research and Development Laboratories:
2-Chloro-3-methoxybenzaldehyde is commonly used in research and development laboratories for its role in the synthesis of new compounds and the exploration of its potential applications in various fields. Its versatility and reactivity make it an essential tool for scientists and researchers working on the development of new materials and products.

Check Digit Verification of cas no

The CAS Registry Mumber 54881-49-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,8 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 54881-49:
(7*5)+(6*4)+(5*8)+(4*8)+(3*1)+(2*4)+(1*9)=151
151 % 10 = 1
So 54881-49-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H7ClO2/c1-11-7-4-2-3-6(5-10)8(7)9/h2-5H,1H3

54881-49-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-3-Methoxybenzaldehyde

1.2 Other means of identification

Product number -
Other names 2-chloro-3-methoxybenzaldehyde

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:54881-49-1 SDS

54881-49-1Relevant articles and documents

Stereoselective Synthesis of the Benzodihydropentalene Core of the Fijiolides

Kurzawa, Timon,Harms, Klaus,Koert, Ulrich

, p. 1388 - 1391 (2018)

An efficient stereoselective synthesis of the enantiomer of the benzodihydropentalene core of fijiolides A and B has been achieved. The asymmetric conjugate addition of styrylboronic acid to an indenone produced the first stereocenter. Ring C was installe

Stereoselective isomerizations of 4-(2′-chloro-3′-methoxyphenyl)-2,5-dimethyl-1,3-dioxolanes: Stereochemistry and conformation of the product 2-benzopyrans

Giles, Robin G. F.,Green, Ivan R.,Li, Shuk-Hui

, p. 565 - 571 (2005)

Stereoselective isomerization of rel-(2R,4S,5R)-4-(2′-chloro-3′-methoxyphenyl)-2,5-dimethyl-1, 3-dioxolane 5 with titanium(IV) chloride afforded solely rel-(1R,3R,4S)-5-chloro-4-hydroxy-6-methoxy-1,3-dimethyl-2-benzopyran 17 in high yield in which the con

BRUTON'S TYROSINE KINASE INHIBITORS

-

, (2017/08/30)

Bruton's tyrosine kinase (Btk) inhibitors have the following Formula (I).

ALKOXY PYRAZOLES AS SOLUBLE GUANYLATE CYCLASE ACTIVATORS

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Paragraph 0116; 0117, (2014/03/25)

The present invention relates to compounds of formula (I): and pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, R5, R6 and R7 are as defined herein. The inventi

DIHYDROPYRIDINE DERIVATIVES

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Page/Page column 10, (2009/09/07)

The present invention relates to dihydropyridine derivatives having general formula (I) or a pharmaceutically acceptable salt thereof, wherein R1 is (1-6C)alkyl, (2-6C)alkenyl, (2-6C)alkynyl, phenyl, (1-5C)heteroaryl R2, R3 are independently (1-4C)alkyl, (2-4C)alkenyl, (2-4C)alkynyl, (1-4C)alkoxy, (24C)alkenyloxy, (2-4C)alkynyloxy, halogen X is SO2, CH2, C(O) or X is absent R4 is (1-6C)alkyl, (2-6C)alkenyl, (2-6C)alkynyl, (3-6C)cycloalkyl, (3-6C)cycloalkenyl, (3-6C)cycloalkyl(1-4C)alkyl, (2-6C)heterocycloalkyl, (2-6C)heterocycloalkyl(14C)alkyl, (6-1 OC)aryl, (6-10C)aryl(1-4C)alkyl, (1-9C)heteroaryl or (1-9C)heteroaryl(14C)alkyl. The compounds are useful for the treatment of fertility disorders.

BICYCLONONENE DERIVATIVES AS RENIN INHIBITORS

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Page/Page column 41-42, (2008/06/13)

The invention relates to novel bicyclononene derivatives of Formula (I); and the use thereof as active ingredients in the preparation of pharmaceutical compositions. The invention also concerns related aspects including processes for the preparation of the compounds, pharmaceutical compositions containing one or more of those compounds and especially their use as inhibitors of renin.

DIHYDROPYRIDINE DERIVATIVES

-

Page/Page column 25-26, (2008/06/13)

The present invention relates to dihydropyridine derivatives having general formula (I) or a pharmaceutically acceptable salt thereof, wherein R1 is (1-6C)alkyl, (2-6C)alkenyl, (2-6C)alkynyl, phenyl, (1-5C)heteroaryl R2, R3 are independently (1-4C)alkyl, (2-4C)alkenyl, (2-4C)alkynyl, (1-4C)alkoxy, (2-4C)alkenyloxy, (2-4C)alkynyloxy, halogen X is SO2, CH2, C(O) or X is absent R4 is (1-6C)alkyl, (2-6C)alkenyl, (2-6C)alkynyl, (3-6C)cycloalkyl, (3-6C)cycloalkenyl, (3-6C)cycloalkyl(1-4C)alkyl, (2-6C)heterocycloalkyl, (2-6C)heterocycloalkyl(1-4C)alkyl, (6-1 OC)aryl, (6-10C)aryl(1-4C)alkyl, (1-9C)heteroaryl or (1-9C)heteroaryl(1-4C)alkyl. The compounds are useful for the treatment of fertility disorders.

PYRIMIDINE-2,4-DIONE DERIVATIVES AS GONADOTROPIN-RELEASING HORMONE RECEPTOR ANTAGONISTS

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Page 30-31, (2008/06/13)

GnRH receptor antagonists are disclosed that have utility in the treatment of a variety of sex-hormone related conditions in both men and women. The compounds of this invention have the structure formula (I) wherein R1a, R1b, R2a, R2b, R3, R4, R5, R6, R7 and X are as defined herein, including stereoisomers, prodrugs and pharmaceutically acceptable salts thereof. Also disclosed are compositions containing a compound of this invention in combination with a pharmaceutically acceptable carrier, as well as methods relating to the use thereof for antagonizing gonadotropin-releasing hormone in a subject in need thereof.

PYRIMIDINE-2, 4-DIONE DERIVATIVES AS GONADOTROPIN-RELEASING HORMONE RECEPTOR ANTAGONISTS

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Page 46, (2010/02/10)

GnRH receptor antagonists are disclosed that have utility in the treatment of a variety of sex-hormone related conditions in both men and women. The compounds of this invention have the structure: wherein R1a, R1b, R1c, R2a, R2b, R3, R4, R5, R6 and X are as defined herein, including stereoisomers, prodrugs and pharmaceutically acceptable salts thereof. Also disclosed are compositions containing a compound of this invention in combination with a pharmaceutically acceptable carrier, as well as methods relating to the use thereof for antagonizing gonadotropin-releasing hormone in a subject in need thereof.

GONADOTROPIN-RELEASING HORMONE RECEPTOR ANTAGONISTS AND METHODS RELATING THERETO

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Page 33, (2010/02/10)

GnRH receptor antagonists are disclosed that have utility in the treatment of a variety of sex-hormone related conditions in both men and women. The compounds of this invention have the structure: wherein n, R1a, R1b, R1c, R2a, R2b, R3, R4, R5, R6 and X are as defined herein, including stereoisomers, prodrugs and pharmaceutically acceptable salts thereof. Also disclosed are compositions containing a compound of this invention in combination with a pharmaceutically acceptable carrier, as well as methods relating to the use thereof for antagonizing gonadotropin-releasing hormone in a subject in need thereof.

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