Fmoc-O-tert-butyl-L-threonine

• CAS: 71989-35-0
• Catalog Number: ACM71989350
• Category: Other Products
• Molecular Weight: 397.46
• Molecular Formula: C₂₃H₂₇NO₅
• Synonyms: 9-FLUORENYLMETHOXYCARBONYL-O-T-BUTYL-L-THEONINE;9-FLUORENYLMETHOXYCARBONYL-O-T-BUTYL-L-THREONINE;FMOC-O-TERT-BUTYL-L-THREONINE;FMOC-O-T-BUTYL-L-THREONINE;FMOC-L-THR(O-T-BUTYL);FMOC-L-THREONINE(O-T-BUTYL);FMOC-L-THREONINE (TBU);FMOC-L-THREONINE T-BUTYL ETHER
• Melting Point: 131-134°C
• Hazard Statements: Xi,N
• Safety Description: 24/25-36/37/39-27-26-61-60
• Supplemental Hazard Statements: H315-H319-H335
• Symbol: GHS07

Custom Q&A

What is the molecular formula of Fmoc-O-tert-butyl-L-threonine?

The molecular formula is C23H27NO5.

What is the molecular weight of Fmoc-O-tert-butyl-L-threonine?

The molecular weight is 397.5 g/mol.

What is the IUPAC name of Fmoc-O-tert-butyl-L-threonine?

The IUPAC name is (2S,3R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[(2-methylpropan-2-yl)oxy]butanoic acid.

What is the InChI of Fmoc-O-tert-butyl-L-threonine?

The InChI is InChI=1S/C23H27NO5/c1-14(29-23(2,3)4)20(21(25)26)24-22(27)28-13-19-17-11-7-5-9-15(17)16-10-6-8-12-18(16)19/h5-12,14,19-20H,13H2,1-4H3,(H,24,27)(H,25,26)/t14-,20+/m1/s1.

What is the InChIKey of Fmoc-O-tert-butyl-L-threonine?

The InChIKey is LZOLWEQBVPVDPR-VLIAUNLRSA-N.

What is the CAS number of Fmoc-O-tert-butyl-L-threonine?

The CAS number is 71989-35-0.

What is the EC number of Fmoc-O-tert-butyl-L-threonine?

The EC number is 276-261-1.

What is the Monoisotopic Mass of Fmoc-O-tert-butyl-L-threonine?

The Monoisotopic Mass is 397.18892296 g/mol.

How many hydrogen bond donor counts are there in Fmoc-O-tert-butyl-L-threonine?

There are 2 hydrogen bond donor counts.

How many rotatable bond counts are there in Fmoc-O-tert-butyl-L-threonine?

There are 8 rotatable bond counts.

Synthetic Use

Upstream Synthesis Route 1

• 4378-13-6
• 102774-86-7

• 71989-35-0

Reference: [1] Liebigs Annalen der Chemie, 1988, p. 1095 - 1098

Downstream Synthesis Route 1

• 71989-35-0

• 4378-13-6

Reference: [1] Amino Acids, 2014, vol. 46, # 2, p. 367 - 374
[2] Patent: WO2012/136604, 2012, A1, . Location in patent: Page/Page column 42

Downstream Synthesis Route 2

• 71989-35-0

• 4425-82-5
• 4378-13-6

Reference: [1] Chimia, 2010, vol. 64, # 3, p. 200 - 202

* For details of the synthesis route, please refer to the original source to ensure accuracy.