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157427-46-8

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157427-46-8 Usage

General Description

N-Methylindole-2-tributylstannane is a specialized chemical compound, which comprises of its root compound, 'indole', with a methyl group attached, and also features the element tin (stannane) in its structure. This chemical compound belongs to a class of organometallic compounds called organotin compounds. They are not naturally occurring and are generally synthesized in laboratory settings for their use in various applications. The specifics of its utilization can largely vary depending on the context, which could range from organic synthesis to use in potential pharmaceutical products. N-Methylindole-2-tributylstannane must be handled with appropriate safety measures as organotin compounds can be harmful or toxic.

Check Digit Verification of cas no

The CAS Registry Mumber 157427-46-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,4,2 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 157427-46:
(8*1)+(7*5)+(6*7)+(5*4)+(4*2)+(3*7)+(2*4)+(1*6)=148
148 % 10 = 8
So 157427-46-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N.3C4H9.Sn/c1-10-7-6-8-4-2-3-5-9(8)10;3*1-3-4-2;/h2-6H,1H3;3*1,3-4H2,2H3;/rC21H35NSn/c1-5-8-15-23(16-9-6-2,17-10-7-3)21-18-19-13-11-12-14-20(19)22(21)4/h11-14,18H,5-10,15-17H2,1-4H3

157427-46-8 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H51515)  1-Methyl-2-(tri-n-butylstannyl)indole, 96%   

  • 157427-46-8

  • 1g

  • 1285.0CNY

  • Detail
  • Aldrich

  • (719366)  N-Methyl-2-(tributylstannyl)indole  97%

  • 157427-46-8

  • 719366-1G

  • 1,208.61CNY

  • Detail

157427-46-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Methylindole-2-tributylstannane

1.2 Other means of identification

Product number -
Other names tributyl-(1-methylindol-2-yl)stannane

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:157427-46-8 SDS

157427-46-8Relevant articles and documents

Iodine-Mediated Intramolecular Dehydrogenative Coupling: Synthesis of N-Alkylindolo[3,2-c]- and -[2,3-c]quinoline Iodides

Volvoikar, Prajesh S.,Tilve, Santosh G.

, p. 892 - 895 (2016)

An I2/TBHP-mediated intramolecular dehydrogenative coupling reaction is developed for the synthesis of a library of medicinally important 5,11-dialkylindolo[3,2-c]quinoline salts and 5,7-dimethylindolo[2,3-c]quinoline salts. The annulation reaction is followed by aromatization to yield tetracycles in good yield. This protocol is also demonstrated for the synthesis of the naturally occurring isocryptolepine in salt form.

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