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N-TERT-BUTYL-3-METHYL-2-BUTENALDIMINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56637-64-0

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56637-64-0 Usage

Chemical Properties

clear colorless liquid

Check Digit Verification of cas no

The CAS Registry Mumber 56637-64-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,3 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56637-64:
(7*5)+(6*6)+(5*6)+(4*3)+(3*7)+(2*6)+(1*4)=150
150 % 10 = 0
So 56637-64-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H17N/c1-8(2)6-7-10-9(3,4)5/h6-7H,1-5H3/b10-7+

56637-64-0SDS

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-TERT-BUTYL-3-METHYL-2-BUTENALDIMINE

1.2 Other means of identification

Product number -
Other names tert-butylimine of dimethylacrylaldehyde

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:56637-64-0 SDS

56637-64-0Relevant academic research and scientific papers

A new prenylation method using β-methyl-γ-trimethylsilyl-N-tert-butylcrotonaldimine

Bellassoued, Moncef,Salemkour, Malika

, p. 115 - 124 (2007/10/03)

A γ-condensation of the silylated imine 2 with carbonyl compounds was achieved in DMSO at room temperature and in the presence of CsF as catalyst; δ-hydroxyenals 6 and dihydro-2H-pyranols 7 were obtained.However, when the reaction was carried out at 100 d

A New and Easy Synthesis of Diethyl 2-Formylalkylphosphonates

Teulade, Marie-Paule,Savignac, Philippe

, p. 1037 - 1039 (2007/10/02)

Aldimines obtained from 2-alkenals are condensed with triethyl phosphite in ethanol in the presence of formic acid to give diethyl iminoalkylphosphonates; these are readily converted into diethyl formylalkylphosphonates in acidic medium.

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