1. Home
  2. Acetic acid, cyano[[(1,1-dimethylethoxy)carbonyl]amino]-,1,1-dimethylethyl ester

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Acetic acid, cyano[[(1,1-dimethylethoxy)carbonyl]amino]-,1,1-dimethylethyl ester

N#CC(C(=O)OC(C)(C)C)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: Acetic acid, cyano[[(1,1-dimethylethoxy)carbonyl]amino]-,1,1-dimethylethyl ester
CAS Number: 130892-40-9
Product Number: AG00HSA0(AGN-PC-0PJC1F)
Synonyms:
MDL No:
Molecular Formula: C12H20N2O4
Molecular Weight: 256.2982

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The tert-Butyl 2-((tert-butoxycarbonyl)amino)-2-cyanoacetate is a versatile compound widely utilized in chemical synthesis. This specific compound plays a crucial role in organic chemistry as a key building block for the synthesis of various complex organic molecules. Due to its unique structure and reactivity, it is commonly used as a protecting group for the amino function in peptide synthesis.In chemical synthesis, tert-Butyl 2-((tert-butoxycarbonyl)amino)-2-cyanoacetate serves as a valuable intermediate in the preparation of peptides and other biologically active compounds. By selectively masking the amino group with the tert-butoxycarbonyl (Boc) protecting group, this compound facilitates the manipulation of amino acids during peptide assembly. This protection strategy ensures the preservation of the desired reactivity of the other functional groups present in the molecule, allowing for controlled and precise chemical transformations.Furthermore, tert-Butyl 2-((tert-butoxycarbonyl)amino)-2-cyanoacetate can participate in various chemical reactions, such as nucleophilic substitutions, condensation reactions, and cyclizations, enabling the synthesis of diverse organic compounds. Its compatibility with a wide range of reaction conditions and functional groups makes it a valuable tool in the hands of synthetic chemists striving to access complex molecular architectures efficiently and selectively.