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36929-60-9

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36929-60-9 Usage

Description

1-METHYL-1H-PYRROLE-3-CARBALDEHYDE, also known as 1-pyrroline-3-carbaldehyde, is a chemical compound characterized by the molecular formula C6H7NO. It is a colorless to pale yellow liquid with a distinctive odor.
Used in Fragrance Industry:
1-METHYL-1H-PYRROLE-3-CARBALDEHYDE is used as a fragrance ingredient for its distinctive scent, contributing to the production of perfumes and colognes.
Used in Pharmaceutical Industry:
1-METHYL-1H-PYRROLE-3-CARBALDEHYDE is used as a key component in the synthesis of various pharmaceuticals, playing a crucial role in the development of new medications.
Used in Food Industry:
1-METHYL-1H-PYRROLE-3-CARBALDEHYDE is used as a flavoring agent to enhance the taste and aroma of different food products.
Used in Dye Manufacturing:
1-METHYL-1H-PYRROLE-3-CARBALDEHYDE is used in the manufacturing of dyes, contributing to the coloration and quality of various products.
Used as a Chemical Intermediate:
1-METHYL-1H-PYRROLE-3-CARBALDEHYDE is utilized as an intermediate in a range of chemical reactions, facilitating the production of diverse chemical compounds.
It is important to handle 1-METHYL-1H-PYRROLE-3-CARBALDEHYDE with care due to its flammable nature and potential to cause irritation to the skin, eyes, and respiratory system.

Check Digit Verification of cas no

The CAS Registry Mumber 36929-60-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,9,2 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 36929-60:
(7*3)+(6*6)+(5*9)+(4*2)+(3*9)+(2*6)+(1*0)=149
149 % 10 = 9
So 36929-60-9 is a valid CAS Registry Number.

36929-60-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methylpyrrole-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 3-formyl-1-methylpyrrole

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:36929-60-9 SDS

36929-60-9Relevant articles and documents

Photo-on-Demand Synthesis of Vilsmeier Reagents with Chloroform and Their Applications to One-Pot Organic Syntheses

Liang, Fengying,Eda, Kazuo,Okazoe, Takashi,Wada, Akihiro,Mori, Nobuaki,Konishi, Katsuhiko,Tsuda, Akihiko

, p. 6504 - 6517 (2021/05/06)

The Vilsmeier reagent (VR), first reported a century ago, is a versatile reagent in a variety of organic reactions. It is used extensively in formylation reactions. However, the synthesis of VR generally requires highly toxic and corrosive reagents such as POCl3, SOCl2, or COCl2. In this study, we found that VR is readily obtained from a CHCl3 solution containing N,N-dimethylformamide or N,N-dimethylacetamide upon photo-irradiation under O2 bubbling. The corresponding Vilsmeier reagents were obtained in high yields with the generation of gaseous HCl and CO2 as byproducts to allow their isolations as crystalline solid products amenable to analysis by X-ray crystallography. With the advantage of using CHCl3, which bifunctionally serves as a reactant and a solvent, this photo-on-demand VR synthesis is available for one-pot syntheses of aldehydes, acid chlorides, formates, ketones, esters, and amides.

REDUCTIONS OF 3-(N-ARYLAMINOMETHYLENE)SUCCINIMIDES

Abramovitch, Rudolph A.,Chapman, Andrew V.

, p. 89 - 92 (2007/10/02)

The reduction Z-N-methylanilinomethylene-N'-phenylsuccinimide is reported and, depending on the conditions, a variety of products may be formed in reasonable yield.For example, the regioselectivity of the NaBH4/EtOH reduction is different from that predicted in the literature, and LAH reduction under mild conditions gives N-phenylpyrrole-3-carboxaldehyde.

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