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159990-12-2

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159990-12-2 Usage

Uses

(S)-3-((tert-Butoxycarbonyl)amino)-3-(4-methoxyphenyl)propanoic Acid is used as a reactant in the preparation of carnosine derivatives as selective and efficient sequestering agents of cytotoxic reactive carbonyl species.

Check Digit Verification of cas no

The CAS Registry Mumber 159990-12-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,9,9 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 159990-12:
(8*1)+(7*5)+(6*9)+(5*9)+(4*9)+(3*0)+(2*1)+(1*2)=182
182 % 10 = 2
So 159990-12-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H21NO5/c1-15(2,3)21-14(19)16-12(9-13(17)18)10-5-7-11(20-4)8-6-10/h5-8,12H,9H2,1-4H3,(H,16,19)(H,17,18)/t12-/m0/s1

159990-12-2 Well-known Company Product Price

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  • Aldrich

  • (69456)  (S)-Boc-4-methoxy-β-Phe-OH  ≥98.0% (HPLC)

  • 159990-12-2

  • 69456-500MG-F

  • 3,535.74CNY

  • Detail

159990-12-2SDS

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 (S)-3-((tert-Butoxycarbonyl)amino)-3-(4-methoxyphenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names (3S)-3-(4-methoxyphenyl)-3-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid

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:159990-12-2 SDS

159990-12-2Relevant articles and documents

Total Synthesis of 2'-Deoxymugineic Acid and Nicotianamine

Matsuura, Fumiyoshi,Hamada, Yasumasa,Shioiri, Takayuki

, p. 9457 - 9470 (2007/10/02)

Steroselective total synthesis of the unique phytosiderophores, 2'-deoxymugineic acid (4) and nicotianamine (5), has been achieved from the β-tyrosine derivative 21 using its aryl groups as the carboxyl synthon.

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