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N-tert-butylhexanamide is a chemical compound with the molecular formula C12H25NO. It is a white crystalline solid that is soluble in organic solvents. This amide is formed by the condensation of hexanoic acid and tert-butylamine, resulting in a compound with potential applications in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its structure features a hexane chain with an amide group at one end and a tert-butyl group at the other, which can influence its physical and chemical properties, such as solubility and reactivity. N-tert-butylhexanamide is an example of a secondary amide, which can undergo hydrolysis to yield the corresponding carboxylic acid and amine.

1190-31-4

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1190-31-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1190-31-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1190-31:
(6*1)+(5*1)+(4*9)+(3*0)+(2*3)+(1*1)=54
54 % 10 = 4
So 1190-31-4 is a valid CAS Registry Number.

1190-31-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-[(3S,8S,9S,10R,13S,14S,16R,17S)-3-hydroxy-10,13,16-trimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-oxoethyl] acetate

1.2 Other means of identification

Product number -
Other names N-tert-butylcaproamide

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:1190-31-4 SDS

1190-31-4Downstream Products

1190-31-4Relevant academic research and scientific papers

Intermolecular hydrogen bonding between N-substituted caproamides and tetrahydrofuran

Jovic,Nikolic,Hollo

, p. 431 - 436 (2013)

The results are reported of a study of hydrogen bonding between various N-substituted caproamides and tetrahydrofuran as an O-electron donor by means of FTIR spectroscopy. The spectroscopic characteristics for N-H.O hydrogen bonded complexes are given. The B3LYP functional with 6-31G**basis set has been used to calculate the structural parameters of the studied hydrogen bonded complexes. It can be assumed that both inductive and steric effects play an important role in the stability of these hydrogen bonded complexes.

Weak base-promoted selective rearrangement of oxaziridines to amidesviavisible-light photoredox catalysis

Park, Jin,Park, Sehoon,Jang, Gwang Seok,Kim, Ran Hui,Jung, Jaehoon,Woo, Sang Kook

, p. 9995 - 9998 (2021/10/06)

The selective rearrangement of oxaziridines to amidesviaa single electron transfer (SET) pathway is unexplored. In this study, we present a weak base-promoted selective rearrangement of oxaziridines to amidesviavisible-light photoredox catalysis. The developed method shows excellent functional group tolerance with a broad substrate scope and good to excellent yields. Furthermore, control experiments and density functional theory (DFT) calculations are performed to gain insight into the reactivity and selectivity.

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