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102-49-8

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102-49-8 Usage

Description

3,4-Dichlorobenzylamine is a benzylamine compound, which belongs to a class of small-molecule compounds with simple structures. These compounds are widely found in the biological world and possess significant physiological and pharmacological activities. They are extensively utilized in the research and development of antibacterial drugs, with a clear colorless to light yellow liquid appearance.

Uses

Used in Pharmaceutical Industry:
3,4-Dichlorobenzylamine is used as a key component in the development of antibacterial drugs due to its potent physiological and pharmacological properties. It contributes to the creation of effective medications that target various bacterial infections.
Used in Antifungal Applications:
In the field of antifungal drugs, 3,4-Dichlorobenzylamine is used as a structural element in the synthesis of drugs like terbinafine and butenafine. These medications are designed to combat fungal infections effectively, providing relief and treatment to patients suffering from such conditions.
Used in Research and Development:
3,4-Dichlorobenzylamine is also employed in the research and development sector, where it aids in the discovery and innovation of new drugs with enhanced antibacterial and antifungal properties. Its presence in the biological world and its significant physiological and pharmacological activities make it a valuable asset in the scientific community.

Check Digit Verification of cas no

The CAS Registry Mumber 102-49-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 102-49:
(5*1)+(4*0)+(3*2)+(2*4)+(1*9)=28
28 % 10 = 8
So 102-49-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H7Cl2N/c8-6-2-1-5(4-10)3-7(6)9/h1-3H,4,10H2/p+1

102-49-8 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (L04899)  3,4-Dichlorobenzylamine, 96%   

  • 102-49-8

  • 5g

  • 428.0CNY

  • Detail
  • Alfa Aesar

  • (L04899)  3,4-Dichlorobenzylamine, 96%   

  • 102-49-8

  • 25g

  • 1446.0CNY

  • Detail

102-49-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-Dichlorobenzylamine

1.2 Other means of identification

Product number -
Other names (3,4-Dichlorophenyl)methanamine

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:102-49-8 SDS

102-49-8Relevant articles and documents

Ultra-small cobalt nanoparticles from molecularly-defined Co-salen complexes for catalytic synthesis of amines

Beller, Matthias,Chandrashekhar, Vishwas G.,Gawande, Manoj B.,Jagadeesh, Rajenahally V.,Kalevaru, Narayana V.,Kamer, Paul C. J.,Senthamarai, Thirusangumurugan,Zbo?il, Radek

, p. 2973 - 2981 (2020/03/27)

We report the synthesis of in situ generated cobalt nanoparticles from molecularly defined complexes as efficient and selective catalysts for reductive amination reactions. In the presence of ammonia and hydrogen, cobalt-salen complexes such as cobalt(ii)-N,N′-bis(salicylidene)-1,2-phenylenediamine produce ultra-small (2-4 nm) cobalt-nanoparticles embedded in a carbon-nitrogen framework. The resulting materials constitute stable, reusable and magnetically separable catalysts, which enable the synthesis of linear and branched benzylic, heterocyclic and aliphatic primary amines from carbonyl compounds and ammonia. The isolated nanoparticles also represent excellent catalysts for the synthesis of primary, secondary as well as tertiary amines including biologically relevant N-methyl amines.

A benzylamine synthetic method of the compound (by machine translation)

-

Paragraph 0044; 0045; 0046, (2018/09/11)

The invention discloses a compound of formula (V) indicated by the benzylamine compound synthetic methods: shown in formula (IV) of the phenmethyl nitrine as raw materials, in the boron tribromide, solvent A and gas B under the protection of the reduction reaction, after the reaction, the solvent C quenching, after treatment [...] (V) indicated by the benzylamine compound. Compared with the existing method, the invention adopts the mild reaction conditions of boron tribromide reagent, avoid the use of a metal catalyst, the operation is simple, the reaction yield is high. (by machine translation)

MOF-derived cobalt nanoparticles catalyze a general synthesis of amines

Jagadeesh, Rajenahally V.,Murugesan, Kathiravan,Alshammari, Ahmad S.,Neumann, Helfried,Pohl, Marga-Martina,Radnik, J?rg,Beller, Matthias

, p. 326 - 332 (2017/09/28)

The development of base metal catalysts for the synthesis of pharmaceutically relevant compounds remains an important goal of chemical research. Here, we report that cobalt nanoparticles encapsulated by a graphitic shell are broadly effective reductive amination catalysts. Their convenient and practical preparation entailed template assembly of cobaltdiamine- dicarboxylic acid metal organic frameworks on carbon and subsequent pyrolysis under inert atmosphere.The resulting stable and reusable catalysts were active for synthesis of primary, secondary, tertiary, and N-methylamines (more than 140 examples).The reaction couples easily accessible carbonyl compounds (aldehydes and ketones) with ammonia, amines, or nitro compounds, and molecular hydrogen under industrially viable and scalable conditions, offering cost-effective access to numerous amines, amino acid derivatives, and more complex drug targets.

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