Product
Supplier
Encyclopedia
Inquiry
Home > Encyclopedia > N-(tert-Butoxycarbonyl)-L-glutamic acid 1-tert-butyl ester

N-(tert-Butoxycarbonyl)-L-glutamic acid 1-tert-butyl ester

N-(tert-Butoxycarbonyl)-L-glutamic acid 1-tert-butyl ester structure

N-(tert-Butoxycarbonyl)-L-glutamic acid 1-tert-butyl ester 

structure
  • CAS No:

    24277-39-2

  • Formula:

    C14H25NO6

  • Chemical Name:

    N-(tert-Butoxycarbonyl)-L-glutamic acid 1-tert-butyl ester

  • Synonyms:

    L-Glutamic acid,N-[(1,1-dimethylethoxy)carbonyl]-,1-(1,1-dimethylethyl) ester;Glutamic acid,N-carboxy-,N,1-di-tert-butyl ester,L-;N-tert-Butoxycarbonylglutamic acid α-tert-butyl ester;NSC 164659;N-(tert-Butoxycarbonyl)-L-glutamic acid 1-tert-butyl ester;639: PN: WO2006034056 TABLE: 10 claimed protein;(4S)-5-tert-Butoxy-4-[(tert-butoxycarbonyl)amino]-5-oxopentanoic acid;BOC-L-glutamic acid tert-butyl ester;N-α-tert-Butoxycarbonyl-L-glutamic acid α-tert butyl ester;(S)-5-tert-Butoxy-4-(tert-butoxycarbonylamino)-5-oxopentanoic acid;N-Boc-glutamic acid tert-butyl ester;(S)-2-[(tert-Butoxycarbonyl)amino]pentanedioic acid 1-tert-butyl ester;Boc-L-glutamic acid 1-tert-butyl ester;(4S)-5-(tert-Butoxy)-4-[[(tert-butoxy)carbonyl]amino]-5-oxopentanoic acid;(4S)-5-[(2-Methylpropan-2-yl)oxy]-4-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxopentanoic acid;500297-64-3

  • Categories:

    Biochemical Engineering  >  Amino Acids and Derivatives

Description

White powder crystal

N-(tert-Butoxycarbonyl)-L-glutamic acid 1-tert-butyl ester Basic Attributes

303.35

303.35

164659

29241900

Characteristics

102

1.7

1.1±0.1 g/cm3

103.3-105.5 °C

449.8°C at 760 mmHg

225.8±27.3 °C

1.470

soluble in dimethyl formamide.

−20°C

Safety Information

NONH for all modes of transport

3

22/22-36/37/38

4-7-28-35-44

N-(tert-Butoxycarbonyl)-L-glutamic acid 1-tert-butyl ester Use and Manufacturing

Solution of crude N-Boc-Glutamic acid 1-tert-butyl ester, 5-methyl ester from the previous step (30.4 g, 95.8 mmol) in THF (300 mL) was mixed with 144 mL of IN LiOH. After 40 minutes of stirring, TLC showed absence of starting material. THF was removed on a roto-vap. Aqueous solution was extracted with AcOEt (3×100 mL) and acidified to pH 4 with solid citric acid. The mixture was extracted again with AcOEt (3×100 mL). Acetate extracts from acidic extraction were combined, washed with brine (2×50 mL), dried (MgSOGeneral procedure: 0.2 N solution of LiOH (38 mL, 7.6 mmol) was added to a solution of 6.9 mmol of N-Boc-diester 10 or 11 in 38 mL of THF cooled to 0 °C. The mixture was stirred at 0 °C for 30 min, then for 20 h at room temperature. The solution was evaporated by half, 20 mL of 5 percent aqueous solution of NaHCO

Computed Properties

Molecular Weight:303.35
XLogP3:1.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:9
Exact Mass:303.16818752
Monoisotopic Mass:303.16818752
Topological Polar Surface Area:102
Heavy Atom Count:21
Complexity:391
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Recommended Suppliers of N-(tert-Butoxycarbonyl)-L-glutamic acid 1-tert-butyl ester

Scan the QR Code to Share

Feedback & Suggestions
Send Message

Thank you for your feedback. If you require further assistance, please contact us by email at info@echemi.com or call us at +86-532-55729510.