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38161-09-0

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38161-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38161-09-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,1,6 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 38161-09:
(7*3)+(6*8)+(5*1)+(4*6)+(3*1)+(2*0)+(1*9)=110
110 % 10 = 0
So 38161-09-0 is a valid CAS Registry Number.

38161-09-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-di(propan-2-yl)butanamide

1.2 Other means of identification

Product number -
Other names Butyryl-di-isopropyl-amid

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:38161-09-0 SDS

38161-09-0Downstream Products

38161-09-0Relevant articles and documents

Iridium-Catalyzed Enantioselective Unbiased Methylene C(sp3)–H Borylation of Acyclic Amides

Yang, Yuhuan,Chen, Lili,Xu, Senmiao

supporting information, p. 3524 - 3528 (2020/12/15)

We herein report amide directed enantioselective β-C(sp3)?H borylation of unbiased methylene C?H bonds of acyclic amides enabled by iridium catalysis for the first time. The key to the success of this transformation relies on the careful select

Catalytic acylation of amines with aldehydes or aldoximes

Allen, C. Liana,Davulcu, Simge,Williams, Jonathan M. J.

supporting information; experimental part, p. 5096 - 5099 (2011/02/21)

The simple nickel salt NiCl2?6H2O catalyzes the coupling of aldoximes with amines to give secondary or tertiary amide products. The aldoxime can be prepared in situ from the corresponding aldehyde. The use of 18O-labeled oximes has allowed insight into the mechanism of this reaction.

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