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2-(4-nitrophenyl)propan-2-amine, also known as 4-Methyl-2-nitrophenethylamine, is a chemical compound with the molecular formula C9H11NO2. It is a primary amine and a derivative of phenethylamine. 2-(4-nitrophenyl)propan-2-aMine has a molecular weight of 165.19 g/mol and a melting point of 112-113°C. It is commonly used in the synthesis of various pharmaceuticals and organic compounds. This chemical is known to have potential pharmacological properties and may have applications in the development of new drugs and medicines.

3276-37-7

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3276-37-7 Usage

Uses

Used in Pharmaceutical Industry:
2-(4-nitrophenyl)propan-2-amine is used as a key intermediate in the synthesis of various pharmaceuticals for its potential pharmacological properties. It plays a crucial role in the development of new drugs and medicines, contributing to the advancement of healthcare.
Used in Organic Chemistry:
2-(4-nitrophenyl)propan-2-amine is used as a building block in the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of molecules with diverse applications in different industries, such as agriculture, materials science, and more.

Check Digit Verification of cas no

The CAS Registry Mumber 3276-37-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,7 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3276-37:
(6*3)+(5*2)+(4*7)+(3*6)+(2*3)+(1*7)=87
87 % 10 = 7
So 3276-37-7 is a valid CAS Registry Number.

3276-37-7SDS

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 2-(4-nitrophenyl)propan-2-amine

1.2 Other means of identification

Product number -
Other names 2-<4-Nitro-phenyl>-2-amino-propan

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:3276-37-7 SDS

3276-37-7Relevant academic research and scientific papers

3-PHOSPHOGLYCERATE DEHYDROGENASE INHIBITORS AND USES THEREOF

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Paragraph 00441, (2017/10/06)

The present invention provides compounds, compositions thereof, and methods of using the same.

3. 4 - diphenyl - 4H - 1, 2, 4 - triazole derivative and its preparation method and application (by machine translation)

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Paragraph 0415; 0423; 0424; 0425, (2017/07/01)

The invention discloses 3, 4 - diphenyl - 4H - 1, 2, 4 - triazole derivative and its preparation method and application. In particular, the invention relates to the formula (I) structure of 3, 4 - diphenyl - 4H - 1, 2, 4 - triazole derivatives, its stereoisomers or its pharmaceutically acceptable salt, formula (I) in the definition of each substituent is as defined in the specification. These structure of novel compound with heat shock protein HSP90 inhibitory activity, can be used for treating cancer, neurodegenerative diseases, inflammatory diseases, autoimmune diseases, ischemic brain injury and the like, it has broad application prospects. (by machine translation)

Substituted alkylamine derivatives and methods of use

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Page 93, (2010/02/05)

Selected amines are effective for prophylaxis and treatment of diseases, such as angiogenesis mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable salts thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving, cancer and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.

1,5-benzodiazepine compounds, their production and use

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, (2008/06/13)

A compound represented by the formula (I) [wherein ring B represents a cyclic hydrocarbon group which may have substituent(s); Z represents hydrogen atom or a cyclic group which may have substituent(s); R1 represents hydrogen atom, a hydrocarbon group which may have substituent(s), a heterocyclic group which may have substituent(s) or an acyl group; R2 represents amino group which may have substituent(s); D represents a bond or a divalent group; E represents a bond, —CO—, —CON(Ra)—, —COO—, —N(Ra)CON(Rb)—, —N(Ra)COO—, —N(Ra)SO2—, —N(Ra)—, —O—, —S—, —SO— or —SO2— (Ra and Rb each independently represents hydrogen atom or a hydrocarbon group which may have substituent(s)); G represents a bond or a divalent group; L represents a bond or a divalent group; A represents hydrogen atom or a substituent; X and Y each represents hydrogen atom or an independent substituent; and . . . represents that R2 and an atom on ring B may form a ring] or a salt thereof, and a process for producing the same.

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