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1008562-87-5

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1008562-87-5 Usage

General Description

(S)-tert-Butyl 3-formylpiperidine-1-carboxylate is a chemical compound with the molecular formula C13H23NO3. It is a piperidine derivative with a tert-butyl group and a formyl group attached to the piperidine ring. (S)-tert-Butyl 3-formylpiperidine-1-carboxylate is commonly used in organic synthesis as a building block for the preparation of various pharmaceuticals and other complex organic molecules. It has been reported to exhibit antiproliferative activity against cancer cells and has potential applications in drug development. (S)-tert-Butyl 3-formylpiperidine-1-carboxylate is a versatile intermediate in organic chemistry and is of interest to researchers in the fields of medicinal chemistry and chemical biology.

Check Digit Verification of cas no

The CAS Registry Mumber 1008562-87-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,8,5,6 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1008562-87:
(9*1)+(8*0)+(7*0)+(6*8)+(5*5)+(4*6)+(3*2)+(2*8)+(1*7)=135
135 % 10 = 5
So 1008562-87-5 is a valid CAS Registry Number.

1008562-87-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-3-formyl-piperidine-1-carboxylic acid tert-butyl ester

1.2 Other means of identification

Product number -
Other names (S)-TERT-BUTYL 3-FORMYLPIPERIDINE 1-CARBOXYLATE

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:1008562-87-5 SDS

1008562-87-5Relevant articles and documents

Access to 1,3-Dinitriles by Enantioselective Auto-tandem Catalysis: Merging Allylic Cyanation with Asymmetric Hydrocyanation

Fang, Xianjie,Gao, Jihui,Long, Jinguo,Yu, Rongrong

, p. 6785 - 6789 (2020)

Enantioselective auto-tandem catalysis represents a challenging yet highlight attractive topic in the field of asymmetric catalysis. In this context, we describe a dual catalytic cycle that merges allylic cyanation and asymmetric hydrocyanation. The one-pot conversion of a broad array of allylic alcohols into their corresponding 1,3-dinitriles proceeds in good yield with high enantioselectivity. The products are densely functionalized and can be easily transformed to chiral diamines, dinitriles, diesters, and piperidines. Mechanistic studies clearly support a novel sequential cyanation/hydrocyanation pathway.

MODULATORS OF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR

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Paragraph 00938, (2021/02/19)

This disclosure provides modulators of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR), pharmaceutical compositions containing at least one such modulator, methods of treatment of cystic fibrosis using such modulators and pharmaceutical compositions, and processes for making such modulators.

15-PGDH INHIBITOR

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Paragraph 0471-0472, (2021/12/23)

[Problem] To provide a compound having a 15-PGDH inhibitory effect. [Solution] A compound represented by general formula (1) or a pharmacologically acceptable salt thereof.

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