ChemicalBook > Product Catalog >Biochemical Engineering >Amino Acids and Derivatives >Phenylalanine derivatives >BOC-L-4-Nitrophe

BOC-L-4-Nitrophe

BOC-L-4-Nitrophe  Structure
CAS No.
33305-77-0
Chemical Name:
BOC-L-4-Nitrophe
Synonyms
Phe(4-NO2);D-Phe.otBu.HCl;BOC-L-4-NITROPHE;BOC-L-PHE(4-NO2);BOC-PHE(4''-NO2);Boc-4-NO2-Phe-OH;BOC-(P-NO2)PHE-OH;BOC-PNO2-L-PHE-OH;BOC-PHE(4-NO2)-OH;BOC-PHE(P-NO2)-OH
CBNumber:
CB0178783
Molecular Formula:
C14H18N2O6
Molecular Weight:
310.3
MOL File:
33305-77-0.mol
Modify Date:
2023/10/8 21:24:08

BOC-L-4-Nitrophe Properties

Melting point 107°C
alpha 8 º (c=1,MeOH)
Boiling point 509.3±45.0 °C(Predicted)
Density 1.290±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility Chloroform (Slightly), Ethanol (Slightly)
form Solid
pka 3.70±0.10(Predicted)
color Pale Beige
optical activity [α]20/D +8±1°, c = 1% in methanol
BRN 2820671
InChIKey XBQADBXCNQPHHY-NSHDSACASA-N
CAS DataBase Reference 33305-77-0

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS05
Signal word  Warning
Hazard statements  H314
Precautionary statements  P264b-P271-P280-P301+P330+P331-P304+P340-P305+P351+P338-P310-P363-P403+P233-P501c
Hazard Codes  Xi
Safety Statements  24/25
WGK Germany  3
HazardClass  IRRITANT
HS Code  29242990
NFPA 704
1
0 0

BOC-L-4-Nitrophe price More Price(11)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 15348 Boc-Phe(4-NO2)-OH ≥99.0% (T) 33305-77-0 1G ₹3269.15 2022-06-14 Buy
Sigma-Aldrich(India) 15348 Boc-Phe(4-NO2)-OH ≥99.0% (T) 33305-77-0 5G ₹16313.28 2022-06-14 Buy
TCI Chemicals (India) B2232 N-(tert-Butoxycarbonyl)-4-nitro-L-phenylalanine 33305-77-0 1G ₹2900 2022-05-26 Buy
ALFA India ALF-H51986-MD N-Boc-4-nitro-L-phenylalanine, 95% 33305-77-0 250mg ₹1879 2022-05-26 Buy
ALFA India ALF-H51986-06 N-Boc-4-nitro-L-phenylalanine, 95% 33305-77-0 5g ₹5121 2022-05-26 Buy
Product number Packaging Price Buy
15348 1G ₹3269.15 Buy
15348 5G ₹16313.28 Buy
B2232 1G ₹2900 Buy
ALF-H51986-MD 250mg ₹1879 Buy
ALF-H51986-06 5g ₹5121 Buy

BOC-L-4-Nitrophe Chemical Properties,Uses,Production

Chemical Properties

Light yellow powder

Uses

N-Boc-p-nitro-L-phenylalanine is the N-Boc protected form of p-Nitro-L-phenylalanine (N502725, Hydrate) and is a useful synthetic intermediate in the synthesis of Hydroxymelphalan (H939850); an analog of Melphalan (M216900) which is an antineoplastic.

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BOC-PNO2-L-PHE-OH BOC-(P-NO2)PHE-OH BOC-P-NITRO-PHENYLALANINE BOC-P-NITRO-PHE-OH BOC-PHE(P-NO2)-OH BOC-PHE(4-NO2)-OH BOC-L-4-NITROPHE BOC-L-4-NITROPHENYLALANINE BOC-L-PHE(4-NO2) BOC-L-PHE(4-NO2)-OH BOC-4-NITRO PHENYLALANINE BOC-4-NITRO-PHE-OH BOC-4-NITRO-L-PHENYLALANINE N-(tert-Butyloxycarbonyl)-4-nitro-L-phenylalanine Boc-L-4-NO2-Phe-OH Boc-4-Nitro-L-Phenylalanine N-Boc-4-nitro-L-phenylalanine Boc-Phe(4-NO2)-OH (S)-2-t-butyloxycarbonylaMino-3-(4-nitrophenyl)propionic acid H-Phe(4'-NO2)-OBut·HCl Boc-D-4-Nitro-Phe-OH D-Phe.otBu.HCl L-Phenylalanine,N-[(1,1-diMethylethoxy)carbonyl]-4-nitro- (S)-Boc-2-amino-3-(4-nitrophenyl)propionic acid Boc-4-nitro-L-phenylalanine≥ 99% (HPLC) Boc-p-nitro-L-Phe-OH (S)-2-(TERT-BUTOXYCARBONYLAMINO)-3-(4-NITROPHENYL)PROPANOIC ACID RARECHEM BK PT 0074 N-TERT-BUTOXYCARBONYL-4-NITRO-L-PHENYLALANINE N-TBOC-P-NITRO-L-PHENYLALANINE N-ALPHA-T-BUTOXYCARBONYL-(4-NITROPHENYL)-L-ALANINE N-ALPHA-T-BOC-4-NITRO-L-PHENYLALANINE N-ALPHA-TERT-BUTYLOXYCARBONYL-4-NITRO-L-PHENYLALANINE N-ALPHA-T-BUTOXYCARBONYL-P-NITRO-L-PHENYLALANINE N-BOC-4-NITRO-L-PHENYLALANINE N-(tert-butoxycarbonyl)-4-nitro-3-phenyl-L-alanine N-T-BOC-P-NITRO-L-PHENYLALANINE*FREE ACI D 4-Nitro-L-phenylalanine, N-BOC protected N-ALPHA-T-BUTYLOXYCARBONYL-4-NITRO-L-PHENYLALANINE Boc-L-4-NO2-Phe-OH NALPHA-tert-Butoxycarbonyl-3-(4-nitrophenyl)-L-alanine tert-Butoxycarbonyl-L-4-nitrophenylalanine BOC-PHE(4''-NO2) N-TERT-BOC-P-NITRO-L-PHENYLALANINE N-Boc-4-nitro-L-phenylalanine, 95%, BOC-4-Nitro-L-Phenylalanine extrapure, 98% Boc-4-nitro-l-phenylalanine, 98%+ BOC-L-4-Nitrophe USP/EP/BP N-(tert-Butoxycarbonyl)-4-nitro-L-phenylalanine> N-Boc-p-nitro-L-phenylalanine Phe(4-NO2) (Tert-Butoxy)Carbonyl Phe(4-NO2)-OH Boc-4-NO2-Phe-OH Boc-Phe(4-NO2)-OH 33305-77-0 Peptide Synthesis Phenylalanine Derivatives Specialty Synthesis Unnatural Amino Acid Derivatives Boc-Amino acid series