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Benzamide, 3-butyl-N,N-diethyl-2-(trimethylsilyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

141807-38-7

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141807-38-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141807-38-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,8,0 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 141807-38:
(8*1)+(7*4)+(6*1)+(5*8)+(4*0)+(3*7)+(2*3)+(1*8)=117
117 % 10 = 7
So 141807-38-7 is a valid CAS Registry Number.

141807-38-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-butyl-N,N-diethyl-2-(trimethylsilyl)benzamide

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:141807-38-7 SDS

141807-38-7Downstream Products

141807-38-7Relevant academic research and scientific papers

Ni(0)-Catalyzed Cross Coupling of Aryl O-Carbamates and Aryl Triflates with Grignard Reagents. Directed Ortho Metalation-Aligned Synthetic Methods for Polysubstituted Aromatics via a 1,2-Dipole Equivalent

Sengupta, Saumitra,Leite, Magda,Raslan, Delio Soares,Quesnelle, Claude,Snieckus, Victor

, p. 4066 - 4068 (2007/10/02)

The first Ni(0)-catalyzed cross-coupling reactions of aryl O-carbamates and aryl triflates with Grignard reagents (Scheme I) to give diversely polysubstituted aromatics 2d and 2e (Table I) which feature regiospecificity based on directed ortho metalation (carbamate), minimal β-hydride elimination (triflate), and dependence on steric and electronic effects are described.

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