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1-propanamine, 2-methyl-N-(2-methylpropyl)-, hydrobromide (1:1) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74299-56-2

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74299-56-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74299-56-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,9 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74299-56:
(7*7)+(6*4)+(5*2)+(4*9)+(3*9)+(2*5)+(1*6)=162
162 % 10 = 2
So 74299-56-2 is a valid CAS Registry Number.

74299-56-2SDS

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 2-methyl-N-(2-methylpropyl)propan-1-amine,hydrobromide

1.2 Other means of identification

Product number -
Other names diisobutyl-amine,hydrobromide

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:74299-56-2 SDS

74299-56-2Downstream Products

74299-56-2Relevant academic research and scientific papers

Strong Improper Ferroelasticity and Weak Canted Ferroelectricity in a Martensitic-Like Phase Transition of Diisobutylammonium Bromide

Piecha-Bisiorek, Anna,Bia?oska, Agata,Jakubas, Ryszard,Zieliski, Piotr,Wojciechowska, Martyna,Ga?zka, Miros?aw

, p. 5023 - 5027 (2015)

Diisobutylammonium bromide is found to be a unique improper ferroelastic in which the elastic degrees of freedom seem to play the essential role, giving rise to a domain pattern resembling that of martensitic phase transitions. A weak canted ferroelectricity turns out switchable by an electric field.

KINETICS AND MECHANISM OF REACTION OF AMINES WITH β-BROMOPROPIOPHENONE

Popov, A. F.,Piskunova, Z.,Matvienko, V. N.

, p. 1299 - 1302 (2007/10/02)

The reaction of β-bromopropiophenone with different amines in acetonitrile at 25 deg C was studied.It was found that in the case of primary and secondary amines, the end products of the reaction are β-aminopropiophenones, which form via the intermediate phenyl vinyl ketone.In the case of tertiary amines, the reaction ends at the stage of the formation of phenyl vinyl ketone.The reactivity of the amines in the formation of phenyl vinyl ketone is preferentially determined by their basicity.

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