Boc-D-Valine
Boc-D-Valine Basic information
- Product Name:
- Boc-D-Valine
- Synonyms:
-
- N-Boc-D-valine, 98+%
- BOC-D-VALINE extrapure
- BOC-D-VALINE, 98+%
- N-a-t-Boc-D-valine
- N-t-Boc-D-valine
- t-Butoxycarbonyl-D-va
- S-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic aci
- N-Boc-D-valine Boc-D-Val-OH
- CAS:
- 22838-58-0
- MF:
- C10H19NO4
- MW:
- 217.26
- EINECS:
- 1533716-785-6
- Product Categories:
-
- Valine [Val, V]
- Boc-Amino Acids and Derivative
- Amino Acids
- Amino Acids (N-Protected)
- Biochemistry
- Boc-Amino Acids
- Boc-Amino acid series
- Amino Acid Derivatives
- Mol File:
- 22838-58-0.mol
Boc-D-Valine Chemical Properties
- Melting point:
- 164-165 °C
- alpha
- 6.25 º (c=1, acetic acid)
- Boiling point:
- 357.82°C (rough estimate)
- Density
- 1.1518 (rough estimate)
- refractive index
- 6 ° (C=1, AcOH)
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- solubility
- DMSO, Methanol
- form
- Solid
- pka
- 4.01±0.10(Predicted)
- color
- White
- BRN
- 2050408
- Major Application
- peptide synthesis
- InChI
- InChI=1S/C10H19NO4/c1-6(2)7(8(12)13)11-9(14)15-10(3,4)5/h6-7H,1-5H3,(H,11,14)(H,12,13)/t7-/m1/s1
- InChIKey
- SZXBQTSZISFIAO-SSDOTTSWSA-N
- SMILES
- C(O)(=O)[C@@H](C(C)C)NC(OC(C)(C)C)=O
- CAS DataBase Reference
- 22838-58-0(CAS DataBase Reference)
Safety Information
- Safety Statements
- 24/25
- WGK Germany
- 3
- HS Code
- 29241990
- Storage Class
- 11 - Combustible Solids
MSDS
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
Boc-D-Valine Usage And Synthesis
Chemical Properties
White to off-white powder
Uses
tert-Butoxycarbonyl-D-valine is used in the preparation of selective CCR1 antagonists in the treatment of rheumatoid arthritis. Also used in the preparation of antileishmanial agents.
reaction suitability
reaction type: Boc solid-phase peptide synthesis
Synthesis
D-Valine, 20 mL of ethyl acetate and 10 mL of tetrahydrofuran were added to the reaction bottle, 4.2 g (19.3 mmol) of Boc anhydride was added to the reaction system, and stirred at room temperature for 6 h. The progress of the reaction was detected by thin-layer chromatography, and waited for the end of the reaction. The reaction solution was evaporated to dryness, and saturated ammonium chloride solution was added to the residual solution to separate the organic phase, which was then washed with saturated saline, dried, filtered and evaporated to dryness to obtain Boc-D-valine.
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Boc-D-Valine(22838-58-0)Related Product Information
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- Boc-L-Glutamic acid 5-benzylester
- BOC-D-PHE-OSU
- 1-BOC-D-PYROGLUTAMIC ACID ETHYL ESTER
- Methyl N-(tert-butoxycarbonyl)-L-threoninate
- Boc-Hyp-OH
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- BOC-GUANIDINE
- N-Boc-L-valine
- BOC-D-ALPHA-T-BUTYLGLYCINE
- Boc-alpha-Cyclohexyl-D-glycine
- Boc-D-isoleucine