CAS 102123-74-0
:N-Boc phenylalanyl chloride
Description:
N-Boc phenylalanyl chloride is a chemical compound that serves as an important intermediate in organic synthesis, particularly in the field of peptide chemistry. It features a phenylalanine residue protected by a tert-butyloxycarbonyl (Boc) group, which is a common protective group used to shield amines during chemical reactions. The presence of the chloride functional group indicates that it can participate in nucleophilic substitution reactions, making it useful for coupling reactions in peptide synthesis. This compound is typically a white to off-white solid and is soluble in organic solvents such as dichloromethane and ethyl acetate. It is important to handle N-Boc phenylalanyl chloride with care, as it can be reactive and may pose hazards if not managed properly. The compound is often utilized in the preparation of various peptides and can be involved in the development of pharmaceuticals and biologically active molecules. As with all chemical substances, appropriate safety measures should be taken when handling and storing this compound.
Formula:C15H20ClNO3
InChI:InChI=1/C15H20ClNO3/c1-15(2,3)20-14(19)17-12(13(18)10-16)9-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,17,19)/t12-/m0/s1
InChI key:InChIKey=JAKDNFBATYIEIE-LBPRGKRZSA-N
SMILES:[C@@H](CC1=CC=CC=C1)(NC(OC(C)(C)C)=O)C(CCl)=O
Synonyms:- (3S)-(-)-3-tert-Butoxycarbonylamino-1-chloro-4-phenyl-2-butanone
- (3S)-3-(N-Boc-amino)-1-chloro-4-phenyl-2-butanone
- (S)-tert-Butyl (4-chloro-3-oxo-1-phenylbutan-2-yl)carbamate
- Carbamic acid, N-[(1S)-3-chloro-2-oxo-1-(phenylmethyl)propyl]-, 1,1-dimethylethyl ester
- Carbamic acid, [(1S)-3-chloro-2-oxo-1-(phenylmethyl)propyl]-, 1,1-dimethylethyl ester
- Carbamic acid, [(1S)-3-chloro-2-oxo-1-(phenylmethyl)propyl]-, 1,1-dimethylethyl ester (9CI)
- Carbamic acid, [3-chloro-2-oxo-1-(phenylmethyl)propyl]-, 1,1-dimethylethyl ester, (S)-
- N-Boc phenylalanyl chloride
- tert-butyl [(1S)-1-benzyl-3-chloro-2-oxopropyl]carbamate
- N-(1-chloro-3-oxo-1-phenylbutan-2-yl)carbamic acid tert-butyl ester
- N-[(1S)-3-chloro-2-oxo-1-(phenylMethyl)propyl]-
- N-[(1S)-3-chloro-2-oxo-1-(phenylmethyl)propyl]-Carbamic acid 1,1-dimethylethyl ester
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Found 7 products.
Carbamic acid, N-[(1S)-3-chloro-2-oxo-1-(phenylmethyl)propyl]-, 1,1-dimethylethyl ester
CAS:Formula:C15H20ClNO3Purity:97%Color and Shape:LiquidMolecular weight:297.7772(S)-tert-Butyl (4-chloro-3-oxo-1-phenylbutan-2-yl)carbamate
CAS:(S)-tert-Butyl (4-chloro-3-oxo-1-phenylbutan-2-yl)carbamatePurity:98%Molecular weight:297.78g/mol(S)-tert-Butyl (4-chloro-3-oxo-1-phenylbutan-2-yl)carbamate
CAS:Formula:C15H20ClNO3Purity:97%Color and Shape:SolidMolecular weight:297.78(3S)-3-(tert-Butoxycarbonyl)amino-1-chloro-4-phenyl-2-butanone
CAS:<p>(3S)-3-(tert-Butoxycarbonyl)amino-1-chloro-4-phenyl-2-butanone is an organic compound that belongs to the class of carbonyl reductase. It is used as a catalyst for the transformation of secondary alcohols to ketones or aldehydes, including isopropyl alcohol. The reaction proceeds via an intermediate carboxylic acid. The enzyme has been found in various microorganisms, and can be purified from Bacillus megaterium and Streptomyces lividans. The enzyme’s activity can be inhibited by steric effects, metal ions, or other compounds. (3S)-3-(tert-Butoxycarbonyl)amino-1-chloro-4-phenyl-2-butanone crystallizes in two forms: one with the chiral center at the 3 position and one with it at the 4 position.</p>Purity:Min. 95%






