(4R)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-[(2-methyl-2-propanyl)oxy]-L-proline | CAS No. 122996-47-8

(4R)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-[(2-methyl-2-propanyl)oxy]-L-proline

Basic Information

CAS Number

122996-47-8

Molecular Formula

C24H27NO5

Molecular Weight

409.48 g/mol

AD

Basic Physical Properties

Melting Point

59.0 to 64.0 deg-C

Specific Rotation

-25±2.5° (c=1%,in methanol)

CC(C)(C)OC1CC(N(C1)C(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24)C(=O)O

InChI

InChI=1S/C24H27NO5/c1-24(2,3)30-15-12-21(22(26)27)25(13-15)23(28)29-14-20-18-10-6-4-8-16(18)17-9-5-7-11-19(17)20/h4-11,15,20-21H,12-14H2,1-3H3,(H,26,27)/t15-,21+/m1/s1

InChIKey

WPBXBYOKQUEIDW-VFNWGFHPSA-N

LogP

4.278100000000003

Topological Polar Surface Area

76.07 Ų

Hydrogen Bond Donor/Acceptor

1 / 6

Complexity

622

Safety Information

View Safety Information

Hazard Statement

H315 Causes skin irritation
Skin corrosion/irritation
H319 Causes serious eye irritation
Serious eye damage/eye irritation
H335 May cause respiratory irritation
Specific target organ toxicity, single exposure; Respiratory tract irritation

Hazard Class

Class IRRITANT Class IRRITANT

Synonyms & References

English

  • (2S,4R)-1-(9H-fluoren-9-ylmethoxycarbonyl)-4-[(2-methylpropan-2-yl)oxy]pyrrolidine-2-carboxylic acid
  • F1095
  • fmoc-4-tert-butoxy-l-proline
  • N-alpha-Fmoc-O-tert-butyl-L-trans-4-hydroxyproline
  • J-004880
  • SCHEMBL118220
  • HY-W010964
  • FMOC- Hyp(tBu)- OH
  • AS-17468
  • (2S,4R)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-(tert-butoxy)pyrrolidine-2-carboxylicacid
  • Fmoc-O-tert.butyl-trans-4-hydroxy-L-proline
  • N-Fmoc-4-trans-(tert-butoxy)-L-proline
  • Fmoc-D-Hyp(tBu)-OH
  • Trans-N-Fmoc-4-(tert-butoxy)-L-proline
  • WPBXBYOKQUEIDW-VFNWGFHPSA-N
  • CS-W011680
  • N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-trans-(tert-butoxy)-L-proline
  • Fmoc-(2S,4R)-(-)-4-t-butoxypyrrolidine-2-carboxylic acid
  • Fmoc-O-tert-butyl-L-hydroxyproline
  • (2S,4R)-4-(tert-butoxy)-1-{[(9H-fluoren-9-yl)methoxy]carbonyl}pyrrolidine-2-carboxylic acid
  • Fmoc-Hyp(OtBu)-OH
  • Z2044808427
  • Fmoc-Hyp(tBu)-OH, >=98.0% (HPLC)
  • 1,2-Pyrrolidinedicarboxylic acid, 4-(1,1-dimethylethoxy)-, 1-(9H-fluoren-9-ylmethyl) ester, (2S,4R)-
  • (2S,4R)-4-(tert-butoxy)-1-[(9H-fluoren-9-ylmethoxy)carbonyl]pyrrolidine-2-carboxylic acid
  • Fmoc-L-Hyp(tBu)-OH
  • A20638
  • FD21786
  • AM81837
  • 122996-47-8
  • Fmoc-Hyp(OtBu)OH

MDL Number

MFCD00151930

FAQ

What are the physical and chemical properties of (4R)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-[(2-methyl-2-propanyl)oxy]-L-proline (CAS: 122996-47-8)?

(4R)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-[(2-methyl-2-propanyl)oxy]-L-proline is a crystalline compound with a molecular weight of approximately 494.52 g/mol. It is soluble in organic solvents such as dichloromethane and methanol. The compound shows good reactivity in esterification and amide formation reactions.

How is (4R)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-[(2-methyl-2-propanyl)oxy]-L-proline (CAS: 122996-47-8) typically synthesized?

(4R)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-[(2-methyl-2-propanyl)oxy]-L-proline is typically synthesized via a multi-step process involving the protection of the L-proline with fluorenylmethoxycarbonyl (Fmoc) group, followed by the introduction of the 2-methyl-2-propanol moiety. The synthesis involves the use of catalytic amounts of a suitable reagent and is known to have good yield and selectivity.

What industries use (4R)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-[(2-methyl-2-propanyl)oxy]-L-proline (CAS: 122996-47-8)?

(4R)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-[(2-methyl-2-propanyl)oxy]-L-proline is primarily used in the pharmaceutical industry for the synthesis of complex molecules and in polymer industry for the development of new materials with specific properties.

What precautions should be taken when handling (4R)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-[(2-methyl-2-propanyl)oxy]-L-proline (CAS: 122996-47-8)?

When handling (4R)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-[(2-methyl-2-propanyl)oxy]-L-proline, it is essential to wear appropriate personal protective equipment (PPE), including gloves and safety glasses. The compound should be stored in a cool, dry place away from direct sunlight. In case of spill, neutralize the spill with an appropriate reagent and dispose of the waste according to local regulations. Always refer to the Safety Data Sheet (SDS) for detailed handling and disposal instructions.

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