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Boc-DL-valine

Base Information Edit
  • Chemical Name:Boc-DL-valine
  • CAS No.:54895-12-4
  • Molecular Formula:C10H19NO4
  • Molecular Weight:217.265
  • Hs Code.:29241990
  • NSC Number:334316,197197
  • DSSTox Substance ID:DTXSID40297033
  • Nikkaji Number:J1.513.371F
  • Mol file:54895-12-4.mol
Boc-DL-valine

Synonyms:Boc-DL-valine;54895-12-4;Boc-DL-Val-OH;2-((tert-butoxycarbonyl)amino)-3-methylbutanoic acid;N-BOC-DL-VALINE;BOC-[15N]VAL-OH;N-(tert-butoxycarbonyl)valine;3-methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid;MFCD00069973;2-{[(tert-butoxy)carbonyl]amino}-3-methylbutanoic acid;dl-n-(tert-butoxycarbonyl)valine;2-[(TERT-BUTOXYCARBONYL)AMINO]-3-METHYLBUTANOIC ACID;n-t-boc-valine;NSC-197197;Ethyl2-Nonylacetoacetate;CBMicro_013815;Cambridge id 5211804;2-(tert-butoxycarbonylamino)-3-methylbutanoic acid;SCHEMBL467994;(tert-Butoxycarbonyl)DL-valine;(2R)-3-methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid;DTXSID40297033;Valine, N-tert-butyl ester, L-;SZXBQTSZISFIAO-UHFFFAOYSA-N;SMSF0004505;Boc-DL-Val-OH, >=98.0%;BBL100120;NSC197197;NSC334316;STK367904;L-Valine,1-dimethylethoxy)carbonyl]-;AKOS000167564;AKOS016347234;AB01721;AB02648;AB02811;CB07237;CS-W004861;DS-2298;HY-W004861;NSC-334316;N-(TERT-BUTOXYCARBONYL)-D-VALIN;N-(TERT-BUTOXYCARBONYL)-DL-VALINE;PD195994;SY006036;SY006484;SY007790;BIM-0013768.P001;AM20100353;FT-0629993;FT-0636953;FT-0689488;EN300-29802;2-tert-butoxycarbonylamino-3-methyl-butyric acid;2-((tert-butoxycarbonyl)amino)-3-methylbutanoicacid;2-(tert-Butoxycarbonylamino)-3-methyl-butanoic acid;Q-102754;(SR)-2-tert-butoxycarbonylamino-3-methylbutyric acid;2-[(tert-butoxycarbonyl) amino]-3-methylbutanoic acid;Z285919532;141509-91-3;Boc-Val-OH-15N;L-Valine-15N,N-t-Bocderivative;N-(tert-Butoxycarbonyl)-L-valine-15N

Suppliers and Price of Boc-DL-valine
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • Boc-DL-valine
  • 10g
  • $ 343.00
  • Usbiological
  • Boc-DL-valine 99+%
  • 5g
  • $ 179.00
  • Sigma-Aldrich
  • Boc-DL-Val-OH ≥98.0%
  • 10g
  • $ 83.10
  • Medical Isotopes, Inc.
  • 2-((tert-Butoxycarbonyl)amino)-3-methylbutanoicacid 95+%
  • 10 g
  • $ 340.00
  • Matrix Scientific
  • Boc-DL-Valine >95%
  • 5g
  • $ 46.00
  • Matrix Scientific
  • Boc-DL-Valine >95%
  • 10g
  • $ 72.00
  • Frontier Specialty Chemicals
  • Boc-DL-valine 98%
  • 10g
  • $ 102.00
  • Frontier Specialty Chemicals
  • Boc-DL-valine 98%
  • 50g
  • $ 419.00
  • Crysdot
  • 2-((tert-Butoxycarbonyl)amino)-3-methylbutanoicacid 97%
  • 500g
  • $ 321.00
  • ChemScene
  • 2-((tert-Butoxycarbonyl)amino)-3-methylbutanoicacid
  • 100g
  • $ 59.00
Total 35 raw suppliers
Chemical Property of Boc-DL-valine Edit
Chemical Property:
  • Melting Point:112-114℃ 
  • Boiling Point:341.8 °C at 760 mmHg 
  • PKA:4.01±0.10(Predicted) 
  • Flash Point:160.5 °C 
  • PSA:75.63000 
  • Density:1.079g/cm3 
  • LogP:2.01120 
  • Storage Temp.:Store at RT. 
  • XLogP3:1.5
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:5
  • Exact Mass:217.13140809
  • Heavy Atom Count:15
  • Complexity:242
Purity/Quality:

98%,99%, *data from raw suppliers

Boc-DL-valine *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Safety Statements: 24/25 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)C(C(=O)O)NC(=O)OC(C)(C)C
  • Uses 2-(tert-Butoxycarbonylamino)-3-methylbutanoic Acid is a useful synthesis intermediate used in the preparation of amino acid ester homocamptothecin analogs that exhibits anti-tumor properties.
Technology Process of Boc-DL-valine

There total 11 articles about Boc-DL-valine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With sodium hydroxide; sodium hydrogencarbonate; In 1,4-dioxane; water; at 20 ℃;
DOI:10.1002/ejoc.200400105
Guidance literature:
With triethylamine; In 1,4-dioxane; water; for 0.166667h; Ambient temperature;
DOI:10.1039/c39830001357
Guidance literature:
With sodium acetate; In acetonitrile; for 3h; Electrochemical reaction;
DOI:10.1021/ol005537w
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