ChemicalBook > CAS DataBase List > 2-Chloro-L-phenylalanine

2-Chloro-L-phenylalanine

Product Name
2-Chloro-L-phenylalanine
CAS No.
103616-89-3
Chemical Name
2-Chloro-L-phenylalanine
Synonyms
L-Phe(2-Cl)-OH;CAS:103616-89-3;L-H-Phe(2-Cl)-OH;JACS-103616-89-3;L-2-Chloro-phe-OH;2-CHLORO-PHE-OH HCL;2-Chloro-L-phenylala;2-Chloro-L-phenylalanine;2-CHLORO-PHE-OHHCL 98%MIN;L-Phenylalanine,2-chloro-
CBNumber
CB5104840
Molecular Formula
C9H10ClNO2
Formula Weight
199.63
MOL File
103616-89-3.mol
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2-Chloro-L-phenylalanine Property

Melting point:
233-235°C
Boiling point:
339.5±32.0 °C(Predicted)
Density 
1.336±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
DMSO (Slightly), Water (Slightly)
pka
2.16±0.10(Predicted)
form 
Solid
color 
White to Off-White
Water Solubility 
Insoluble in water.
InChI
InChI=1S/C9H10ClNO2/c10-7-4-2-1-3-6(7)5-8(11)9(12)13/h1-4,8H,5,11H2,(H,12,13)/t8-/m0/s1
InChIKey
CVZZNRXMDCOHBG-QMMMGPOBSA-N
SMILES
C(O)(=O)[C@H](CC1=CC=CC=C1Cl)N
CAS DataBase Reference
103616-89-3(CAS DataBase Reference)
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Safety

Hazard Codes 
Xi
Safety Statements 
24/25
WGK Germany 
3
HS Code 
29224999
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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.

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N-Bromosuccinimide Price

TRC
Product number
C350385
Product name
2-Chloro-L-phenylalanine
Packaging
250mg
Price
$55
Updated
2021/12/16
TRC
Product number
C350385
Product name
2-Chloro-L-phenylalanine
Packaging
500mg
Price
$65
Updated
2021/12/16
Usbiological
Product number
230209
Product name
2-Chloro-L-phenylalanine 99+%
Packaging
1g
Price
$200
Updated
2021/12/16
Usbiological
Product number
269684
Product name
2-Chloro-L-phenylalanine
Packaging
1g
Price
$355
Updated
2021/12/16
Activate Scientific
Product number
AS88010
Product name
2-Chloro-L-phenylalanine
Purity
97+% ee
Packaging
1g
Price
$28
Updated
2021/12/16
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2-Chloro-L-phenylalanine Chemical Properties,Usage,Production

Uses

The largest gain in affinity of all tested unnatural amino acids was observed for 2-chloro-L-phenylalanine.

Definition

ChEBI: 2-Chloro-L-phenylalanine is a phenylalanine derivative.

Synthesis

3752-25-8

103616-89-3

The general steps for the synthesis of L-2-chlorophenylalanine from 2-chlorocinnamic acid were as follows: first, based on the phenylalanine amino lyase (PAL) protein sequence of Rhodosporidium toruloides ATCC 10788 (NCBI Protein Data Bank No. CAA31209), the Genscript Corporation to synthesize the PAL gene of R. glutinis and codon optimized for E. coli expression. The synthesized PAL gene was ligated to the SmaI site of the pUC57 vector by Genscript to construct the pUC57_PAL plasmid. 5 μg of lyophilized pUC57_PAL plasmid was dissolved in 50 μl of MilliQ water, and 1 μl of the solution was taken to transform E. coli DH5α chemoreceptor cells according to the supplier's protocol. The transformed cells were cultured on LB solid medium containing 100 μg/ml carbenicillin at 37°C overnight. Single colonies were selected for inoculation in 20 ml of LB liquid medium containing 100 μg/ml carbenicillin, prepared in 8% glycerol and stored at -80°C. The DH5α strain containing pUC57_PAL was inoculated in 1000 ml of LB medium containing 100 μg/ml carbenicillin and incubated at 28°C overnight. Subsequently, the culture was inoculated in 10 liters of TB medium (containing 0.1 g/l carbenicillin and 1 mM IPTG) and fermented with agitation at 37°C for 9.5 hr at 500 to 1500 rpm. Cells were collected by centrifugation to obtain 230 g of wet cells, which were dispensed into 10 g aliquots stored at -20°C. Prior to the reaction, an appropriate amount of cells was thawed and resuspended in cold water. 1.8 g (10 mmol) of 3-(2-chlorophenyl)-acrylic acid was dissolved in 0.5 L of 13 vol% aqueous ammonia solution, and the pH was adjusted to 11 with 25 w/w% H2SO4. 130 g of wet cells were resuspended in 0.2 L of 13 vol% aqueous ammonia solution of pH 11, mixed with the substrate solution, and the total volume was adjusted to 1 L. The reaction was carried out at 30 °C in a closed 200 rpm vessel. Initially 0.91 g (5.0 mmol) of 3-(2-chlorophenyl)-acrylic acid was added every 5 min for 1 h and the same amount was added every 25 min for the next 7 h. After 8.5 h, the cells were removed by centrifugation and the reaction yield was determined by HPLC to be about 91%, yielding about 18.1 g (91 mmol) of 2-chlorophenylalanine. The supernatant (850 mL, pH 10.8) was concentrated under reduced pressure (150 to 10 mbar, 60 °C) to form a precipitate (pH 7.5) after removal of about 65% water. The precipitate was filtered, washed with water to remove inorganic salts, and dried to give 14.9 g of product containing 57 w/w% N-amino-3-(2-chlorophenyl)-propionic acid (8.5 g, 47% yield), 24 w/w% water, and 1.7 w/w% 3-(2-chlorophenyl)-acrylic acid. The enantiomeric excess (e.e.) of (S)-2-amino-3-(2-chlorophenyl)-propionic acid was 99%. 9.5 g of (S)-2-amino-3-(2-chlorophenyl)-propionic acid remained in the mother liquor.

References

[1] Patent: EP1676838, 2006, A1. Location in patent: Page/Page column 17-18
[2] Patent: WO2006/69799, 2006, A1. Location in patent: Page/Page column 30-31
[3] Journal of the American Chemical Society, 2015, vol. 137, # 40, p. 12977 - 12983
[4] Catalysis Science and Technology, 2016, vol. 6, # 12, p. 4086 - 4089

2-Chloro-L-phenylalanine Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from 2-Chloro-L-phenylalanine manufacturers

Career Henan Chemical Co
Product
2-Chloro-L-phenylalanine 103616-89-3
Price
US $1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
200kg
Release date
2019-12-24

103616-89-3, 2-Chloro-L-phenylalanineRelated Search:


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