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(R)-1-(2,4-DICHLOROPHENYL)ETHANAMINE, with the molecular formula C8H10Cl2N, is a chiral amine characterized by the attachment of a 2,4-dichlorophenyl group to the nitrogen atom. (R)-1-(2,4-DICHLOROPHENYL)ETHANAMINE is of significant interest in both chemical and biological sciences due to its potential applications and biological activity, which is suggested by its structural resemblance to other active amines.

133773-29-2

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133773-29-2 Usage

Uses

Used in Pharmaceutical Synthesis:
(R)-1-(2,4-DICHLOROPHENYL)ETHANAMINE is used as a building block in the synthesis of pharmaceuticals for its potential to contribute to the development of new drugs. Its unique structure allows it to be a key component in creating various organic compounds with therapeutic properties.
Used in Organic Compounds Synthesis:
In the field of organic chemistry, (R)-1-(2,4-DICHLOROPHENYL)ETHANAMINE is utilized as a precursor for synthesizing a range of organic compounds, taking advantage of its reactive sites and structural features to form diverse molecules with specific functions.
Used in Biological Research:
(R)-1-(2,4-DICHLOROPHENYL)ETHANAMINE is employed as a subject of biological research to explore its potential biological activity. Given its structural similarity to other biologically active amines, it may offer insights into the development of new products with applications in medicine and biology.
Used in Drug Development:
(R)-1-(2,4-DICHLOROPHENYL)ETHANAMINE is used as a starting material in drug development, where its unique properties can be leveraged to create novel therapeutic agents. Researchers are interested in its potential to be modified and incorporated into new molecules with specific medicinal uses.

Check Digit Verification of cas no

The CAS Registry Mumber 133773-29-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,7,7 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 133773-29:
(8*1)+(7*3)+(6*3)+(5*7)+(4*7)+(3*3)+(2*2)+(1*9)=132
132 % 10 = 2
So 133773-29-2 is a valid CAS Registry Number.

133773-29-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R)-1-(2,4-Dichlorophenyl)ethanamine

1.2 Other means of identification

Product number -
Other names (R)-2,4-dichloro PEA

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:133773-29-2 SDS

133773-29-2Downstream Products

133773-29-2Relevant academic research and scientific papers

SUBSTITUTED BENZIMIDAZOLES AND BENZOPYRAZOLES AS CCR(4) ANTAGONISTS

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Paragraph 0115, (2013/06/27)

Benzimidazole, benzopyrazole and benzotriazole compounds are provided which bind to CCR(4) and are useful for the treatment of diseases such as allergic diseases, autoimmune diseases, graft rejection and cancer.

SUBSTITUTED ANILINES AS CCR(4) ANTAGONISTS

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Paragraph 0102, (2013/06/27)

Aniline compounds are provided which bind to CCR(4) and are useful for the treatment of diseases such as allergic diseases, autoimmune diseases, graft rejection and cancer.

COMPOSITIONS AND METHODS FOR CYCLOFRUCTANS AS SEPARATION AGENTS

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Page/Page column 45-49; 62, (2010/12/31)

The present invention relates to derivatized cyclofructan compounds, compositions comprising derivatized cyclofructan compounds, and methods of using compositions comprising derivatized cyclofructan compounds for chromatographic separations of chemical species, including enantiomers. Said compositions may comprise a solid support and/or polymers comprising derivatized cyclofructan compounds.

N-(α-alkylbenzylidene)-α-phenylalkylamine, its use and process for producing the same and process for producing intermediate therefor

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, (2008/06/13)

There is disclosed an N-(α-alkylbenzylidene)-α-phenylalkylamine represented by the general formula (1): STR1 wherein R1 represents a lower alkyl group, R2 represents a hydrogen atom, a halogen atom, a lower alkyl group or a lower alkoxy group and X represents a halogen atom or a lower alkoxy group, its use and a process for producing the same and processes for producing intermediates therefor.

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