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188970-92-5

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  • L-Alanine,N-[(9H-fluoren-9-ylmethoxy)carbonyl]-3-[[(2-propen-1-yloxy)carbonyl]amino]-/ LIDE PHARMA- Factory supply / Best price

    Cas No: 188970-92-5

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  • 1000 Kilogram/Day

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188970-92-5 Usage

Description

FMOC-DAP(ALOC)-OH, also known as (S)-3-Allyloxycarbonylamino-2-(Fmoc-amino)propionic acid, is an important organic intermediate with a solid chemical property. It is widely recognized for its versatile applications across various industries due to its unique chemical structure and properties.

Uses

Used in Agrochemical Industry:
FMOC-DAP(ALOC)-OH is used as a key intermediate for the synthesis of various agrochemicals, specifically for the development of novel pesticides and herbicides. Its application in this industry is driven by the need to create more effective and environmentally friendly solutions for crop protection and management.
Used in Pharmaceutical Industry:
FMOC-DAP(ALOC)-OH serves as a crucial building block in the development of new pharmaceutical compounds. It is utilized in the synthesis of innovative drugs and therapies, targeting a wide range of medical conditions. The compound's application in the pharmaceutical industry is attributed to its potential role in enhancing the efficacy and safety of medications.
Used in Dyestuff Industry:
FMOC-DAP(ALOC)-OH is employed as an essential intermediate in the production of various dyes and pigments. Its use in this industry is due to its ability to contribute to the development of new colorants with improved properties, such as enhanced color strength, stability, and environmental sustainability.

Check Digit Verification of cas no

The CAS Registry Mumber 188970-92-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,9,7 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 188970-92:
(8*1)+(7*8)+(6*8)+(5*9)+(4*7)+(3*0)+(2*9)+(1*2)=205
205 % 10 = 5
So 188970-92-5 is a valid CAS Registry Number.
InChI:InChI=1/C22H22N2O6/c1-2-11-29-21(27)23-12-19(20(25)26)24-22(28)30-13-18-16-9-5-3-7-14(16)15-8-4-6-10-17(15)18/h2-10,18-19H,1,11-13H2,(H,23,27)(H,24,28)(H,25,26)/t19-/m0/s1

188970-92-5 Well-known Company Product Price

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  • Alfa Aesar

  • (H63516)  (S)-3-Allyloxycarbonylamino-2-(Fmoc-amino)propionic acid, 95%   

  • 188970-92-5

  • 250mg

  • 377.0CNY

  • Detail
  • Alfa Aesar

  • (H63516)  (S)-3-Allyloxycarbonylamino-2-(Fmoc-amino)propionic acid, 95%   

  • 188970-92-5

  • 1g

  • 1127.0CNY

  • Detail
  • Alfa Aesar

  • (H63516)  (S)-3-Allyloxycarbonylamino-2-(Fmoc-amino)propionic acid, 95%   

  • 188970-92-5

  • 5g

  • 4518.0CNY

  • Detail
  • Aldrich

  • (47546)  Fmoc-Dap(Alloc)-OH  ≥98.5% (HPLC)

  • 188970-92-5

  • 47546-250MG

  • 1,333.80CNY

  • Detail

188970-92-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(prop-2-enoxycarbonylamino)propanoic acid

1.2 Other means of identification

Product number -
Other names Fmoc-L-Dap(Aloc)-OH

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:188970-92-5 SDS

188970-92-5Downstream Products

188970-92-5Relevant articles and documents

Practical and efficient synthesis of orthogonally protected α-2,3-diaminopropionic acid (2,3-Dap), 2,4-diaminobutanoic acid (2,4-Dab), and their N-methylated derivatives

Rao, R. V. Ramana,Tantry, Subramanyam J.,Babu, Vommina V. Suresh

, p. 2901 - 2912 (2007/10/03)

The synthesis of orthogonally protected Fmoc-Dap/Dab (Boc/Z/Alloc)-OH starting from Fmoc-Asp/Glu has been described. The salient features of our synthetic strategy involved formation of Fmoc-Asp/Glu-5-oxazolidinone acids, conversion of acid function to acyl azides, Curtius rearrangement, and hydrolysis of the oxazolidinone group. Copyright Taylor & Francis Group, LLC.

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