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78512-39-7

78512-39-7

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78512-39-7 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 78512-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,5,1 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 78512-39:
(7*7)+(6*8)+(5*5)+(4*1)+(3*2)+(2*3)+(1*9)=147
147 % 10 = 7
So 78512-39-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO4S/c1-12(2,3)17-11(16)13-9(10(14)15)7-8-5-4-6-18-8/h4-6,9H,7H2,1-3H3,(H,13,16)(H,14,15)

78512-39-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-thiophen-2-ylpropanoic acid

1.2 Other means of identification

Product number -
Other names Boc-3-(2-Thienyl)-DL-alanine

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:78512-39-7 SDS

78512-39-7Relevant articles and documents

Studies on Cyclic Dipeptides, I: Aryl Modifications of cyclo-[Phe-His]

Noe,Weigand,Pirker

, p. 1081 - 1097 (2007/10/03)

Seven new cyclic dipeptides have been synthesized and tested for their applicability as tools to elucidate the mechanism of formation of mandelonitrile with (SS)-cyclo-[Phe-His] type catalysts. Conformational analyses based on 1H NMR spectra are presented for all prepared cyclic dipeptides.

RESOLUTION OF β-2-THIENYLALANINE ENANTIOMERS BY A CONVENIENT METHOD

Lipkowski, Andrzej W.,Flouret, George

, p. 2225 - 2228 (2007/10/02)

t-Butyloxycarbonyl derivatives of D- and L-β-2-thienylalanine were prepared by resolution of t-butyloxycarbonyl-D,L-β-2-thienylalanine with (S)- or (R)-α-phenylethylamine.The enantiomeric salts of t-butyloxycarbonyl-amino acids, were converted to t-butylo

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