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N-benzyl-N-methyl-1-(naphthalen-1-yl)methanamine is an organic compound with the molecular formula C20H21N. It is a derivative of methanamine, featuring a naphthalene ring and a benzyl group attached to the nitrogen atom. N-benzyl-N-methyl-1-(naphthalen-1-yl)methanamine is characterized by its unique structure, which includes a methyl group and a naphthalene ring connected to the central methanamine backbone. It is a colorless to pale yellow liquid with a distinct aromatic odor. Due to its complex structure, it is often used in the synthesis of various pharmaceuticals and chemical compounds, particularly those with potential applications in the fields of medicine and materials science. The compound's properties, such as its solubility and reactivity, make it a valuable intermediate in the development of new drugs and other chemical products.

6313-87-7

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6313-87-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6313-87-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6313-87:
(6*6)+(5*3)+(4*1)+(3*3)+(2*8)+(1*7)=87
87 % 10 = 7
So 6313-87-7 is a valid CAS Registry Number.

6313-87-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Benzyl-N-methyl-1-naphthylmethylamin

1.2 Other means of identification

Product number -
Other names -

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

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More Details:6313-87-7 SDS

6313-87-7Downstream Products

6313-87-7Relevant academic research and scientific papers

Cp*Ir complex bearing a flexible bridging and functional 2,2′-methylenebibenzimidazole ligand as an auto-tandem catalyst for the synthesis of N-methyl tertiary amines from imines via transfer hydrogenation/N-methylation with methanol

Ai, Yao,Chen, Xiaozhong,Li, Feng,Liu, Peng,Yang, Chenchen,Yang, Jiazhi

, p. 325 - 334 (2021/10/07)

A Cp*Ir complex bearing a flexible bridging and functional 2,2′-methylenebibenzimidazole ligand was designed, synthesized, and found to be a general and efficient auto-tandem catalyst for the synthesis of N-methyl tertiary amines from imines via transfer hydrogenation/N-methylation with methanol as both hydrogen source and methylating reagent. In the presence of [Cp*Ir(2,2′-CH2BiBzImH2)Cl][Cl], a range of desirable products were obtained in high yields with nearly complete selectivities. The reaction is highly attractive due to the highly atom economy, and minimal consumption of chemicals and energy. Notably, this research exhibits new potential of metal–ligand bifunctional catalysts for the activation of methanol as C1 source for organic synthesis.

Cross-coupling of mesylated phenol derivatives with potassium ammonio-and amidomethyltrifluoroborates

Molander, Gary A.,Beaumard, Floriane

supporting information; experimental part, p. 1242 - 1245 (2011/05/03)

A large array of aryl and heteroaryl mesylates have been successfully employed as electrophiles in a Csp2-Csp3 Suzuki-Miyaura cross-coupling with potassium ammonio-and amidomethyltrifluoroborates to afford the corresponding products

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