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159898-10-9

159898-10-9

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159898-10-9 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 159898-10-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,8,9 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 159898-10:
(8*1)+(7*5)+(6*9)+(5*8)+(4*9)+(3*8)+(2*1)+(1*0)=199
199 % 10 = 9
So 159898-10-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H21NO4/c1-12(2,3)17-11(16)13-7-5-4-6-9(13)8-10(14)15/h9H,4-8H2,1-3H3,(H,14,15)/t9-/m0/s1

159898-10-9 Well-known Company Product Price

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  • Aldrich

  • (669725)  (S)-1-Boc-2-piperidineaceticacid  ≥99.0% (HPLC)

  • 159898-10-9

  • 669725-250MG

  • 1,806.48CNY

  • Detail

  • Aldrich

  • (669725)  (S)-1-Boc-2-piperidineaceticacid  ≥99.0% (HPLC)

  • 159898-10-9

  • 669725-1G

  • 6,312.15CNY

  • Detail

159898-10-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2S)-1-[(2-methylpropan-2-yl)oxycarbonyl]piperidin-2-yl]acetic acid

1.2 Other means of identification

Product number -
Other names 2S-carboxymethyl-piperidine-1-carboxylic acid tert-butyl ester

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:159898-10-9 SDS

159898-10-9Relevant articles and documents

Synthesis of Azocanes from Piperidines via an Azetidinium Intermediate

Leverenz, Malte,Masson, Guillaume,Pardo, Domingo Gomez,Cossy, Janine

, p. 16325 - 16328 (2021/10/25)

α-Trifluoromethyl azocanes are accessible from 2-(trifluoropropan-2-ol) piperidines by metal-free ring-expansion involving a bicyclic azetidinium intermediate. The opening of the azetidinium intermediate was achieved by various nucleophiles (amines, alcoholates, carboxylates, phosphonates, halides and pseudo-halides) with an excellent regio- diastereo- and enantioselectivity and in good yields. The relative configuration of the piperidines and azocanes were assigned and the deprotected azocanes offer opportunities for further derivatization.

Enzymatic resolution of cyclic N-Boc protected β-aminoacids

Pousset, Cyrille,Callens, Roland,Haddad, Mansour,Larcheveque, Marc

, p. 3407 - 3412 (2007/10/03)

Methyl and ethyl esters of N-Boc homoproline, homopipecolic acid and 3-carboxymethyl-morpholine were kinetically resolved by hydrolysis catalysed by Burkholderia cepacia lipase to give the corresponding acids and residual esters in enantiomeric excesses better than 99% (E > 100).

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