BOC-4-IODO-L-PHENYLALANINE

Product Name: BOC-4-IODO-L-PHENYLALANINE
CAS No.: 62129-44-6
Chemical Name: BOC-4-IODO-L-PHENYLALANINE
Synonyms: BOC-L-PHE(4-I);BOC-L-4-IODOPHE;BOC-PHE(4-1)-OH;BOC-PHE(4-I)-OH;BOC-PHE(P-I)-OH;BOC-PI-L-PHE-OH;BOC-4'-IODO-L-PHE;BOC-L-PHE(4-I)-OH;BOC-P-IODO-PHE-OH;BOC-4-IODO-PHE-OH
CBNumber: CB1672091
Molecular Formula: C14H18INO4
Formula Weight: 391.2
MOL File: 62129-44-6.mol

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BOC-4-IODO-L-PHENYLALANINE Property

Melting point:: ~150 °C (dec.)
alpha: 22.5 º (c=1% in ethyl acetate)
Boiling point:: 475.3±40.0 °C(Predicted)
Density: 1.560±0.06 g/cm3(Predicted)
storage temp.: Keep in dark place,Sealed in dry,Room Temperature
solubility: Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form: Powder
pka: 3.84±0.10(Predicted)
optical activity: [α]20/D +22.5±3°, c = 1% in ethyl acetate
Water Solubility: Slightly soluble in water.
Sensitive: Light Sensitive
BRN: 4503851
CAS DataBase Reference: 62129-44-6(CAS DataBase Reference)

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Safety

Hazard Codes: Xi
WGK Germany: 3
F: 8
HazardClass: IRRITANT
HS Code: 2922498590

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P312Call a POISON CENTER or doctor/physician if you feel unwell.

P403+P233Store in a well-ventilated place. Keep container tightly closed.

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 15346
Product name: Boc-Phe(4-I)-OH
Purity: ≥99.0% (TLC)
Packaging: 5g
Price: $55.6
Updated: 2024/03/01

Alfa Aesar

Product number: H51960
Product name: N-Boc-4-iodo-L-phenylalanine, 98%
Packaging: 5g
Price: $104.65
Updated: 2024/03/01

Alfa Aesar

Product number: H51960
Product name: N-Boc-4-iodo-L-phenylalanine, 98%
Packaging: 25g
Price: $390.65
Updated: 2024/03/01

Usbiological

Product number: 262048
Product name: Boc-4-iodo-L-phenylalanine
Packaging: 10g
Price: $470
Updated: 2021/12/16

TRC

Product number: B656695
Product name: Boc-4-iodo-L-phenylalanine
Packaging: 50g
Price: $495
Updated: 2021/12/16

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BOC-4-IODO-L-PHENYLALANINE Chemical Properties,Usage,Production

Chemical Properties

White powder

Uses

N-Boc-4-iodo-L-phenylalanine is used as pharmaceutical intermediate. It is also used as a p-iodo phenyl alanine derivative with N-Boc protection.

BOC-4-IODO-L-PHENYLALANINE Preparation Products And Raw materials

Raw materials

Preparation Products

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BOC-4-IODO-L-PHENYLALANINE Suppliers

China 183 Europe 2 France 2 Germany 6 India 3 Japan 3 Switzerland 2 United Kingdom 10 United States 36 Global 247

Noventek Pharmaceutical Technology Co.,Ltd

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Fax: 0512-
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J & K SCIENTIFIC LTD.

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Meryer (Shanghai) Chemical Technology Co., Ltd.

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Alfa Aesar

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Energy Chemical

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GL Biochem (Shanghai) Ltd

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Capot Chemical Co., Ltd

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View Lastest Price from BOC-4-IODO-L-PHENYLALANINE manufacturers

Career Henan Chemical Co

Product: BOC-D-4-IODOPHENYLALANINE 62129-44-6
Price: US $20.00/KG
Min. Order: 10KG
Purity: 98%
Supply Ability: 100kg
Release date: 2018-07-31

62129-44-6, BOC-4-IODO-L-PHENYLALANINERelated Search:

TERT-BUTYL 4-(BENZYLAMINO)-3-FLUOROPIPERIDINE-1-CARBOXYLATE TERT-BUTYL 4-AMINO-3-FLUOROPIPERIDINE-1-CARBOXYLATE BOC-SAR-OH Boc-N-beta-Trityl-L-asparagine N-tert-Butoxycarbonyl-L-glutamic acid gamma-tert-butyl ester Boc-L-aspartic acid 4-tert-butyl ester Boc-6-AMinocaproic acid BOC-NLE-OH DCHA Succinimido (S)-2-[(tert-butoxycarbonyl)amino]propionate Boc-L-glutamic acid 5-cyclohexyl ester Boc-D-aspartic acid 4-benzyl ester BOC-GLU(OFM)-OH BOC-PHE-SER-ARG-AMC ACETATE SALT BOC-ORN-OH N-Boc-L-alaninol N-Boc-L-Phenylalaninol 4-Iodotoluene 4-IODO-D-PHENYLALANINE

N-ALPHA-T-BUTYLOXYCARBONYL-L-4-IODOPHENYLALANINE

N-alpha-t-Butyloxycarbonyl-4-iodo-L-phenylalanine

BOC-P-IODO-PHENYLALANINE

BOC-P-IODO-PHE-OH

BOC-L-PHE(4-I)

BOC-L-PHE(4-I)-OH

BOC-L-4-IODOLPHENYLALANINE

BOC-L-4-IODOPHE

BOC-L-4-IODOPHENYLALANINE

BOC-4'-IODO-L-PHE

BOC-4-IODO-L-PHENYLALANINE

BOC-4-IODO PHENYLALANINE

BOC-4-IODO-PHE-OH

(S)-N-ALPHA-T-BUTYLOXYCARBONYL-4-IODOPHENYLALANINE

RARECHEM BK PT 0164

(S)-2-(TERT-BUTOXYCARBONYLAMINO)-3-(4-IODOPHENYL)PROPANOIC ACID

N-TBOC-P-IODO-L-PHENYLALANINE

N-ALPHA-T-BUTOXYCARBONYL-4-IODEO-L-PHENYLALANINE

N-ALPHA-T-BUTOXYCARBONYL-P-IODO-L-PHENYLALANINE

N-ALPHA-TERT-BUTYLOXYCARBONYL-L-4-IODOPHENYLALANINE

Boc-4-lodo-Phe-OH

Boc-4-Lodo-L-Phenylalanine

4-Iodo-L-phenylalanine, N-BOC protected

(Tert-Butoxy)Carbonyl Phe(4-I)-OH

4-Iodo-L-phenylalanine, N-BOC protected 98%

N-(tert-butoxycarbonyl)-p-iodo-L-phenylalanine

Boc-L-4-Iodo-phe-OH

(2S)-2-[(tert-Butoxycarbonyl)amino]-3-(4-iodophenyl)propanoic acid

N-(Tert-Butoxycarbonyl)-4-iodo-(L)-phenylalanine

N-Boc-4-Iodo-L-phenylalanine (Boc-Phe(4-I)-OH) ,99% (HPLC)

Boc-L-Phe(4-I) –OH Boc-4-Iodo-L-Phenylalanine

Boc-4-iodo-L-phenylalanine Boc-p-iodo-L-Phe-OH

N-(tert-butyloxycarbonyl)-3-(4-iodophenyl)alanine

(2S)-2-[(tert-Butoxycarbonyl)amino]-3-(4-iodophenyl)propanoic acid, N-(tert-Butoxycarbonyl)-4-iodo-L-phenylalanine

L-N-(tert-Butoxycarbonyl)-4-iodophenylalanine

Boc-Phe(4-I)-OH >=99.0% (TLC)

BOC-S-PHE(4-I)-OH

BOC-(S)-2-AMINO-3-(4'-IODOPHENYL)PROPANOIC ACID

BOC-PHE(4-1)-OH

BOC-PHE(4-I)-OH

BOC-PHE(P-I)-OH

BOC-PI-L-PHE-OH

BOC-P-IODO-L-PHENYLALANINE

BOC-P-IODO-L-PHE-OH

(S)-Boc-2-amino-3-(4-iodophenyl)propionic acid

Boc-4-iodo-L-phenylalanine≥ 98% (HPLC)

(2S)-3-(4-iodophenyl)-2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]propanoic acid

L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-4-iodo-

BOC-4-IODO-L-PHENYLALANINE USP/EP/BP

(2S)-3-(4-iodophenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid

Fampridine Impurity 26 (3-Aminopyridin-4-ol)

62129-44-6

CH33COCONHCHCOOHCH2C6H4I

C14H18IHO4

Specialty Synthesis

Unnatural Amino Acid Derivatives

Phenylalanine Derivatives

Peptide Synthesis