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ETHYL (2R, 3S)-3-BOC-AMINO-2-PIPERIDINEACETATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

150618-13-6

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150618-13-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 150618-13-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,6,1 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 150618-13:
(8*1)+(7*5)+(6*0)+(5*6)+(4*1)+(3*8)+(2*1)+(1*3)=106
106 % 10 = 6
So 150618-13-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H26N2O4/c1-5-19-12(17)9-11-10(7-6-8-15-11)16-13(18)20-14(2,3)4/h10-11,15H,5-9H2,1-4H3,(H,16,18)/t10-,11+/m0/s1

150618-13-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL (2R, 3S)-3-BOC-AMINO-2-PIPERIDINEACETATE

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:150618-13-6 SDS

150618-13-6Upstream product

150618-13-6Relevant academic research and scientific papers

Stereospecific Synthesis of (2R,3S)-3-Amino-2-Piperidineacetic Acid Derivatives for Use as Conformational Constraint in Peptides

Gomez-Monterrey, Isabel,Gonzalez-Muniz, Rosario,Herranz, Rosario,Garcia-Lopez, Teresa

, p. 3593 - 3594 (1993)

Catalytic hydrogenation at 40 deg C of the β-ketoester, obtained from Boc-Orn(Z)-OH and ethyl lithioacetate, provides exclusively ethyl (2R,3S)-3-tert-butyloxycarbonylamino-2-piperidineacetic acid which when suitably protected can be used for peptide synthesis.

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