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27792-82-1

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27792-82-1 Usage

Description

2,3-Dihydro-7-(hydroxymethyl)-1H-pyrrolizin-1-one is a necine base found in the EtOH extract of Urechites karwinskii roots. It is a chemical compound with a unique structure that can be manipulated through chemical reactions, such as reduction and oxidation, to produce different functional groups.

Uses

Used in Chemical Synthesis:
2,3-Dihydro-7-(hydroxymethyl)-1H-pyrrolizin-1-one is used as a starting material for the synthesis of various chemical compounds. The expression is: 2,3-Dihydro-7-(hydroxymethyl)-1H-pyrrolizin-1-one is used as a starting material for [chemical synthesis] for [its unique structure and reactivity].
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,3-Dihydro-7-(hydroxymethyl)-1H-pyrrolizin-1-one is used as an intermediate in the development of new drugs. The expression is: 2,3-Dihydro-7-(hydroxymethyl)-1H-pyrrolizin-1-one is used as an intermediate for [drug development] for [its potential to be modified and incorporated into various drug molecules].
Used in Organic Chemistry Research:
2,3-Dihydro-7-(hydroxymethyl)-1H-pyrrolizin-1-one is also used in organic chemistry research to study the properties and reactions of necine bases and their derivatives. The expression is: 2,3-Dihydro-7-(hydroxymethyl)-1H-pyrrolizin-1-one is used as a subject of study for [organic chemistry research] for [its unique chemical properties and potential for various reactions].

References

Del Castillo et ai., Tetrahedron Lett., 1219 (1970)

Check Digit Verification of cas no

The CAS Registry Mumber 27792-82-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,7,9 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 27792-82:
(7*2)+(6*7)+(5*7)+(4*9)+(3*2)+(2*8)+(1*2)=151
151 % 10 = 1
So 27792-82-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO2/c10-5-6-1-3-9-4-2-7(11)8(6)9/h1,3,10H,2,4-5H2

27792-82-1SDS

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 7-(hydroxymethyl)-2,3-dihydropyrrolizin-1-one

1.2 Other means of identification

Product number -
Other names 7-hydroxymethyl-2,3-dihydro-pyrrolizin-1-one

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:27792-82-1 SDS

27792-82-1Downstream Products

27792-82-1Relevant articles and documents

Synthesis of 2,3-Dihydro-7-hydroxymethyl-1H-pyrrolizin-1-one, the Alkaloid Loroquine

Roeder, Erhard,Bartkowski, Jan-Pit Barko,Bourauel, Thomas

, p. 711 - 714 (2007/10/02)

The title compound 4 is synthesized in 8 steps by cyclization of N-tosylglycinate 5 with vinyl ketone 6.After elimination of water and sulfinic acid the pyrrolecarboxylate 9 is obtained which, on N-alkylation with ethyl acrylate, Dieckmann cyclization, saponification and decarboxylation, yields methylloroquine 12.The reaction with chlorotrimethylsilane/sulfuric acid in acetic anhydride and subsequent saponification gave loroquine (4) in 2.1 percent overall yiels.Key Words: Pheromones / Pyrrolizidine alkaloids / Pyrrolizine / Alkaloids

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