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68471-57-8

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68471-57-8 Usage

General Description

Benzyl 2,3-dihydro-1H-pyrrole-1-carboxylate is a chemical compound with the molecular formula C14H15NO2. It belongs to the class of organic compounds known as esters, which are derived from carboxylic acids. This particular compound is characterized by a benzyl group attached to the nitrogen atom in a pyrrole ring. It has potential applications in the pharmaceutical and chemical industries, where it may be used as a building block or intermediate in the synthesis of other compounds. Additionally, it may also exhibit biological activity and could be the subject of research for its potential pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 68471-57-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,4,7 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 68471-57:
(7*6)+(6*8)+(5*4)+(4*7)+(3*1)+(2*5)+(1*7)=158
158 % 10 = 8
So 68471-57-8 is a valid CAS Registry Number.

68471-57-8 Well-known Company Product Price

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  • Aldrich

  • (740012)  N-Benzyloxycarbonyl-2,3-dihydropyrrole  97%

  • 68471-57-8

  • 740012-1G

  • 758.16CNY

  • Detail

68471-57-8SDS

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 benzyl 2,3-dihydropyrrole-1-carboxylate

1.2 Other means of identification

Product number -
Other names N-Cbz-pyrroline

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:68471-57-8 SDS

68471-57-8Relevant articles and documents

Fragment-oriented synthesis: β-elaboration of cyclic amine fragments using enecarbamates as platform intermediates

Trindade, Alexandre F.,Faulkner, Emily L.,Leach, Andrew G.,Nelson, Adam,Marsden, Stephen P.

, p. 8802 - 8805 (2020/08/17)

A strategy for the β-sp3 functionalisation of cyclic amines is described. Regioselective conversion of protected amines to enecarbamates is achieved through electrochemical oxidation; these intermediates can be derivatised by functionalised alkyl halides under photoredox catalysis. The potential of the methods is highlighted by direct growth of a DCP2B-binding fragment. This journal is

Chiral multi-substituted 4 - hydroxy chroman compound and its preparation method and application

-

Paragraph 0286; 0288, (2017/07/01)

The invention discloses a chiral polysubstituted 4-hydroxychroman compound, and a preparation method and application thereof. The compound has a general structural formula as shown in a formula I which is described in the specification. The preparation method comprises a step of subjecting a salicylaldehyde compound as shown in a general structural formula II and a tertiary alkenyl amide as shown in a general structural formula III to an intermolecular nucleophilic tandem reaction in the presence of a chiral Lewis acid catalyst so as to realize high-efficiency high-selectivity preparation of the chiral polysubstituted 4-hydroxychroman compound. According to the method, the raw material alkenyl amide which can be easily prepared on large scale and the cheap and easily available chiral catalyst are used, and the novel chiral polysubstituted 4-hydroxychroman bicyclo derivative product which cannot be synthesized by using other methods is prepared under mild reaction conditions; and the produce has a stable structure, high yield and enantioselectivity and good application prospects and can be easily separated and purified.

A total synthesis of millingtonine a

Wegner, Jens,Ley, Steven V.,Kirschning, Andreas,Hansen, Anne-Lene,Montenegro Garcia, Javier,Baxendale, Ian R.

supporting information; experimental part, p. 696 - 699 (2012/04/17)

A total synthesis of millingtonine A, a diglycosylated alkaloid, has been accomplished. Millingtonine A possesses a unique racemic tricyclic core structure not known from any other natural or synthetic source until now. The synthesis features a key bond-f

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