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1003560-58-4

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1003560-58-4 Usage

General Description

1-BOC-3-(4-fluorophenyl)-3-hydroxypyrrolidine is a chemical compound with the molecular formula C16H22FNO3. It is a pyrrolidine derivative with a tert-butoxycarbonyl (BOC) protecting group attached to the nitrogen atom. The compound also contains a hydroxy group attached to the pyrrolidine ring and a fluorophenyl substituent attached to the third carbon atom. 1-BOC-3-(4-FLUOROPHENYL)-3-HYDROXYPYRROLIDINE finds applications in organic synthesis and medicinal chemistry, and its unique structure and functional groups make it a valuable building block for the synthesis of various biologically active molecules. Additionally, the presence of the fluorophenyl group also gives this compound potential for use as a fluorescent probe in biological studies.

Check Digit Verification of cas no

The CAS Registry Mumber 1003560-58-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,3,5,6 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1003560-58:
(9*1)+(8*0)+(7*0)+(6*3)+(5*5)+(4*6)+(3*0)+(2*5)+(1*8)=94
94 % 10 = 4
So 1003560-58-4 is a valid CAS Registry Number.

1003560-58-4SDS

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 tert-Butyl 3-(4-fluorophenyl)-3-hydroxypyrrolidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:1003560-58-4 SDS

1003560-58-4Relevant articles and documents

Oxidative Deconstruction of Azetidinols to α-Amino Ketones

Allen, Lewis A. T.,Natho, Philipp,Parsons, Philip J.,Raclea, Robert-Cristian,White, Andrew J. P.

, p. 9375 - 9385 (2020/08/14)

A silver-mediated synthesis of α-amino ketones via the oxidative deconstruction of azetidinols has been developed using a readily scalable protocol with isolated yields up to 80percent. The azetidinols are easily synthesized in one step and can act as protecting groups for these pharmaceutically relevant synthons. Furthermore, mechanistic insights are presented and these data have revealed that the transformation is likely to proceed through the β-scission of an alkoxy radical, followed by oxidation and C-N cleavage of the resulting α-amido radical.

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