1. Home
  2. (S)-tert-Butoxycarbonylamino-(4-chloro-phenyl)-acetic acid

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)-

(S)-tert-Butoxycarbonylamino-(4-chloro-phenyl)-acetic acid

OC(=O)[C@H](c1ccc(cc1)Cl)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: (S)-tert-Butoxycarbonylamino-(4-chloro-phenyl)-acetic acid
CAS Number: 917027-02-2
Product Number: AG006E4V(AGN-PC-0WAJCL)
Synonyms:
MDL No:
Molecular Formula: C13H16ClNO4
Molecular Weight: 285.7234

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Solid

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


(S)-2-((tert-Butoxycarbonyl)amino)-2-(4-chlorophenyl)acetic acid, commonly referred to as $name$, plays a pivotal role in chemical synthesis processes. Its application extends to the field of organic chemistry, where it serves as a versatile building block for the creation of various compounds.One of the key uses of (S)-2-((tert-Butoxycarbonyl)amino)-2-(4-chlorophenyl)acetic acid is in the synthesis of complex molecules and pharmaceutical intermediates. By utilizing its unique structure and properties, chemists can effectively introduce the (S)-2-((tert-Butoxycarbonyl)amino)-2-(4-chlorophenyl)acetic acid moiety into target molecules, thereby influencing their biological activity or physical characteristics.Furthermore, this compound acts as a chiral auxiliary, enabling the control of stereochemistry in asymmetric synthesis. Its presence in chemical reactions can dictate the formation of enantiomerically pure products, a crucial aspect in drug development and other industries where chirality plays a significant role.Overall, (S)-2-((tert-Butoxycarbonyl)amino)-2-(4-chlorophenyl)acetic acid serves as a valuable tool in the hands of synthetic chemists, allowing for the efficient construction of intricate organic compounds with specific stereochemical and functional group patterns.