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Boc-Dab(Aloc)-OH DCHA is a versatile chemical compound used in organic synthesis, derived from 1-(4,4-dimethyl-2,6-dioxabicyclo[3.1.0]hex-3-yl)ethylamine. It is a protected form of Dab(Aloc)-OH, featuring a protective group on the amine group to prevent unwanted reactions during synthesis. Boc-Dab(Aloc)-OH DCHA serves as a valuable building block for the creation of various pharmaceuticals and organic compounds.

327156-92-3

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327156-92-3 Usage

Uses

Used in Pharmaceutical Synthesis:
Boc-Dab(Aloc)-OH DCHA is used as a building block for the synthesis of pharmaceuticals, providing a protected amine group that can be deprotected when needed for further reactions. This feature allows for the controlled assembly of complex molecules with specific therapeutic properties.
Used in Organic Chemistry:
In the field of organic chemistry, Boc-Dab(Aloc)-OH DCHA is utilized as a versatile chemical building block for the synthesis of various organic compounds. Its protected amine group facilitates the construction of intricate molecular structures with precise control over reactivity and selectivity.
Used in Peptide Synthesis:
Boc-Dab(Aloc)-OH DCHA is employed as a key component in peptide synthesis, where its protected amine group allows for the stepwise assembly of peptide chains. The deprotection of the amine group enables the formation of peptide bonds, leading to the synthesis of bioactive peptides and proteins.
Used in Small Molecule Synthesis:
Boc-Dab(Aloc)-OH DCHA is also used in the synthesis of small molecules, where its protected amine group contributes to the formation of diverse molecular architectures. The deprotection step allows for the precise introduction of functional groups, enhancing the compound's reactivity and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 327156-92-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,7,1,5 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 327156-92:
(8*3)+(7*2)+(6*7)+(5*1)+(4*5)+(3*6)+(2*9)+(1*2)=143
143 % 10 = 3
So 327156-92-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H22N2O6.C12H23N/c1-5-8-20-11(18)14-7-6-9(10(16)17)15-12(19)21-13(2,3)4;1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h5,9H,1,6-8H2,2-4H3,(H,14,18)(H,15,19)(H,16,17);11-13H,1-10H2/t9-;/m0./s1

327156-92-3 Well-known Company Product Price

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  • Aldrich

  • (81717)  Boc-Dab(Alloc)-OH(dicyclohexylammonium)salt  ≥99.0% (HPLC)

  • 327156-92-3

  • 81717-1G-F

  • 1,664.91CNY

  • Detail

327156-92-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-cyclohexylcyclohexanamine,(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-(prop-2-enoxycarbonylamino)butanoic acid

1.2 Other means of identification

Product number -
Other names Dicyclohexylamine (S)-4-(((allyloxy)carbonyl)amino)-2-((tert-butoxycarbonyl)amino)butanoate

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:327156-92-3 SDS

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