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19125-76-9

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19125-76-9 Usage

Uses

3-(Dimethylamino)-2-methyl-2-propenal is suitable for use in the synthesis of methylmalondialdehyde.

General Description

Photophysics of 3-dimethylamino-2-methyl-propenal (DMAMP) on excitation to the S2 (ΠΠ*) electronic state using the resonance Raman spectroscopy is reported.

Check Digit Verification of cas no

The CAS Registry Mumber 19125-76-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,2 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19125-76:
(7*1)+(6*9)+(5*1)+(4*2)+(3*5)+(2*7)+(1*6)=109
109 % 10 = 9
So 19125-76-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO/c1-6(5-8)4-7(2)3/h4-5H,1-3H3/b6-4+

19125-76-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-DIMETHYLAMINO-2-METHYL-2-PROPENAL

1.2 Other means of identification

Product number -
Other names 2-Methyl-3-dimethylaminoacrolein

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:19125-76-9 SDS

19125-76-9Relevant articles and documents

TRIISOBUTYLALUMINUM ASSISTED REDUCTIVE REARRANGEMENT OF 2-ETHOXY-4-ALKYL-2,3-DIHYDROFURANS

Menicagli, Rita,Malanga, Corrado,Guidi, Maurizio,Lardicci, Luciano

, p. 171 - 178 (2007/10/02)

The reaction of AlBui3 with the title compounds was investigated.The reductive rearrangement of 2-ethoxy-4-alkyl-2,3-dihydrofurans proceeds in the same way as that of the corresponding dihydropyran compounds although a complete lack of stereocontrol was observed.On the basis of the experimental results obtained, a likely mechanism for this reductive rearrangement is suggested.

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