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15497-51-5

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  • N-METHYL-N-PHENYLBENZOTRIAZOLEMETHAN-AMI NE, MIXTURE OF BT1 & BT2 ISOMERS

    Cas No: 15497-51-5

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15497-51-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15497-51-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,9 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15497-51:
(7*1)+(6*5)+(5*4)+(4*9)+(3*7)+(2*5)+(1*1)=125
125 % 10 = 5
So 15497-51-5 is a valid CAS Registry Number.

15497-51-5 Well-known Company Product Price

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  • Aldrich

  • (465623)  N-Methyl-N-phenylbenzotriazolemethanamine,mixtureofBt1andBt2isomers  

  • 15497-51-5

  • 465623-1G

  • 1,030.77CNY

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15497-51-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(benzotriazol-1-ylmethyl)-N-methylaniline

1.2 Other means of identification

Product number -
Other names (benzotriazolylmethyl)methylphenylamine

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:15497-51-5 SDS

15497-51-5Relevant articles and documents

Regioselective Synthesis of N 2-Alkylated-1,2,3 Triazoles and N 1-Alkylated Benzotriazoles: Cu2S as a Recyclable Nanocatalyst for Oxidative Amination of N, N -Dimethylbenzylamines

Gupta, Sonu,Chandna, Nisha,Singh, Ajai K.,Jain, Nidhi

, p. 3226 - 3235 (2018/03/25)

Copper chalcogenide nanoparticles (Cu2S) synthesized for the first time from a single-source precursor, CuSPh, act as highly efficient and reusable heterogeneous catalyst for regioselective amination of N,N-dimethylbenzylamines with various azo

Reactions of N-Alkyl-N-phenyl-1H-benzotriazole-1-methanamines with α,β-Unsaturated Ethers. A Novel Route to 1,4- and 1,3-Disubstituted 1,2,3,4-Tetrahydroquinolines

Katritzky, Alan R.,Rachwal, Bogumila,Rachwal, Stanislaw

, p. 2588 - 2596 (2007/10/02)

N-Alkyl-N-aryl-1H-benzotriazole-1-methanamines 3, easily accessible from the condensation of anilines with formaldehyde and benzotriazole, undergo acid-catalyzed reactions with ethyl vinyl ether to give 1-alkyl-4-(benzotriazol-1-yl)-1,2,3,4-tetrahydroquin

The Chemistry of N-Substituted Benzotriazoles. Part 14. Novel Routes to Secondary and Tertiary Amines and to N,N-Disubstituted Hydroxylamines

Katritzky, Alan R.,Yannakopoulou, Konstantina,Lue, Ping,Rasala, Danuta,Urogdi, Laszlo

, p. 225 - 233 (2007/10/02)

Tertiary amines of types R4R3CHNR1R2 (2), (R2CH2)2NR1 (10) and 11, or (R2CH2)3N (12), secondary amines of type (R2CH2)2NH (8), and N,N-disubstituted hydroxylamines of type (R2CH2)2NOH (9), are prepared in high yield by the action of Grignard reagents or sodium borohydride on easily available N,N-dialkyl-N-amines (1) or tris(benzotriazolylmethyl)amine (7), on bis(benzotriazolylmethyl)amines (3), (5), and (6), and on N,N-bis(benzotriazolylmethyl)hydroxylamine (4), respectively.

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