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Boc-beta-cyclohexyl-Ala-OH

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Boc-beta-cyclohexyl-Ala-OH Basic information
Product Name:Boc-beta-cyclohexyl-Ala-OH
Synonyms:(S)-2-TERT-BUTOXYCARBONYLAMINO-3-CYCLOHEXYL-PROPIONIC ACID;BOC-L-CYCLOHEXYLALANINE;BOC-L-CHA-OH;BOC-3-CYCLOHEXYL-L-ALANINE;BOC-BETA-CYCLOHEXYL-ALANINE;BOC-CHA-OH;BOC-BETA-CYCLOHEXYL-L-ALANINE;N-T-boc-B-cyclohexyl-L-alanine
CAS:37736-82-6
MF:C14H25NO4
MW:271.35
EINECS:1308068-626-2
Product Categories:Peptide;Amino Acids;pharmacetical
Mol File:37736-82-6.mol
Boc-beta-cyclohexyl-Ala-OH Structure
Boc-beta-cyclohexyl-Ala-OH Chemical Properties
Boiling point 420.4±28.0 °C(Predicted)
density 1.083±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
pka4.02±0.10(Predicted)
form <40°C Solid,>42°C Liquid
AppearanceWhite to off-white <40°C Solid,>42°C Liquid
Optical Rotation[α]20/D 15.5±1°, c = 2% in glacial acetic acid
BRN 3060603
Major Applicationpeptide synthesis
InChIInChI=1/C14H25NO4/c1-14(2,3)19-13(18)15-11(12(16)17)9-10-7-5-4-6-8-10/h10-11H,4-9H2,1-3H3,(H,15,18)(H,16,17)/t11-/s3
InChIKeyMSZQAQJBXGTSHP-NSHDSACASA-N
SMILES[C@H](C(=O)O)(NC(=O)OC(C)(C)C)CC1CCCCC1 |&1:0,r|
CAS DataBase Reference37736-82-6(CAS DataBase Reference)
Safety Information
WGK Germany 3
HazardClass IRRITANT
HS Code 29242990
Storage Class13 - Non Combustible Solids
MSDS Information
Boc-beta-cyclohexyl-Ala-OH Usage And Synthesis
Chemical PropertiesWhite crystalline powder
UsesIt is an agrochemical, organic and pharmaceutical intermediates.
Synthesis
Di-tert-butyl dicarbonate

24424-99-5

H-CHA-OH HCL

25528-71-6

BOC-BETA-CYCLOHEXYL-ALA-OH

37736-82-6

Step 2. Synthesis of (S)-2-((tert-butoxycarbonyl)amino)-3-cyclohexylpropionic acid. (S)-2-amino-3-cyclohexylpropanoic acid hydrochloride (118 g, 0.57 mol) was dissolved in 0.5 N NaOH aqueous solution (1200 mL), followed by the addition of a solution of tetrahydrofuran (THF, 600 mL) of di-tert-butyl dicarbonate (Boc2O, 137 g, 0.63 mol). The reaction mixture was stirred for 2 hours. After completion of the reaction, the organic solvent was removed under reduced pressure. The aqueous phase was washed with ether (Et2O, 2 x 400 mL) to remove unreacted feedstock. Subsequently, the aqueous phase was acidified to pH 5 with aqueous 2 N HCl. The acidified aqueous phase was extracted with ethyl acetate (EtOAc, 3 × 400 mL). The organic phases were combined, washed with saturated brine, dried over anhydrous sodium sulfate (Na2SO4) and concentrated under reduced pressure to give the title compound (S)-2-((tert-butoxycarbonyl)amino)-3-cyclohexylpropanoic acid (142 g, 92%) as an oil.1H NMR (CDCl3) δ: 0.92 (m, 1H), 1.09-1.30 (m, 3H), 1.48 (s, 9H), 1.51 (m, 1H), 1.52 (m, 1H), 1.66 (m, 5H), 1.78 (m, 1H), 4.32 (m, 1H), 4.88 (m, 1H), 8.55-9.48 (br s, 1H).

References[1] Journal of Antibiotics, 1996, vol. 49, # 9, p. 909 - 920
[2] Patent: WO2007/117557, 2007, A2. Location in patent: Page/Page column 91
[3] Patent: US5756763, 1998, A
Boc-beta-cyclohexyl-Ala-OH Preparation Products And Raw materials
Raw materialsDi-tert-butyl dicarbonate-->H-Cha-OH HCl-->Sodium hydroxide-->Tetrahydrofuran-->Hydrochloric acid-->Water
Tag:Boc-beta-cyclohexyl-Ala-OH(37736-82-6) Related Product Information
Boc-D-Abu-OH Boc-Abu-OH Boc-D-Phenylglycine Boc-beta-cyclohexyl-D-alanine monohydrate Boc-L-Cyclohexylglycine (S)-2-((tert-butoxycarbonyl)amino)-4-cyclohexylbutanoic acid Boc-D-Serine Boc-alpha-Cyclohexyl-D-glycine L-Cyclohexylalanine Boc-Cha-OH dcha Boc-Oic-OH Boc-L-cyclohexylalanine hydroxysuccinimide ester Boc-beta-cyclohexyl-Ala-OH Boc-3-cyclohexyl-L-alanine methyl ester (3S,4aR,8aR)-N-Boc-decahydroisoquinoline-3-carboxylic acid (3S,4aS,8aS)-N-Boc-decahydroisoquinoline-3-carboxylic acid Boc-L-cyclohexylalanine 2H2O Boc-L-mecha-OH