(R)-2-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-2-METHYL-HEPT-6-ENOIC ACID - Names and Identifiers
Name | (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-2-methyl-hept-6-enoic acid
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Synonyms | 288617-77-6 Fmoc-alpha-Pentenyl-L-Ala-OH (R)-N-Fmoc-2-(4-pentenyl)alanine (R)-N-Fmoc-2-(4'-pentenyl)alanine Fmoc-(R)-2-amino-2-methylhept-6-enoic acid (R)-2-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-2-METHYL-HEPT-6-ENOIC ACID (R)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-2-Methyl-Hept-6-Enoic acid (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-2-methyl-hept-6-enoic acid (2R)-2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2-methyl-6-heptenoic acid 6-Heptenoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-2-methyl-, (2R)-
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CAS | 288617-77-6
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InChI | InChI=1/C23H25NO4/c1-3-4-9-14-23(2,21(25)26)24-22(27)28-15-20-18-12-7-5-10-16(18)17-11-6-8-13-19(17)20/h3,5-8,10-13,20H,1,4,9,14-15H2,2H3,(H,24,27)(H,25,26)/t23-/m1/s1 |
InChIKey | MRJFPZWLOJOINV-HSZRJFAPSA-N |
(R)-2-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-2-METHYL-HEPT-6-ENOIC ACID - Physico-chemical Properties
Molecular Formula | C23H25NO4
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Molar Mass | 379.45 |
Density | 1.185 |
Boling Point | 591.7±45.0 °C(Predicted) |
Flash Point | 311.671°C |
Vapor Presure | 0mmHg at 25°C |
Appearance | liquid |
Color | pale yellow viscous |
pKa | 3.91±0.41(Predicted) |
Storage Condition | -20°C |
Refractive Index | 1.582 |
(R)-2-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-2-METHYL-HEPT-6-ENOIC ACID - Risk and Safety
Hazard Symbols | N - Dangerous for the environment
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Risk Codes | 50 - Very Toxic to aquatic organisms
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Safety Description | 61 - Avoid release to the environment. Refer to special instructions / safety data sheets.
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UN IDs | UN 3077 9 / PGIII |
WGK Germany | 3 |
TSCA | No |
(R)-2-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-2-METHYL-HEPT-6-ENOIC ACID - Introduction
(2R)-2-(+)-2-methyl-hept-6-enoic is an organic compound with the chemical formula of C21H27NO3 and a molecular weight of 341.45. It possesses two chiral carbon atoms, one of which is the R stereocenter.
This compound is commonly used in chemical synthesis and organic synthesis reactions, especially in the preparation of drugs and biologically active molecules. It can be used as an intermediate for the synthesis of natural products with asymmetric carbon centers or synthetic drugs and other organic molecules.
The method for preparing this compound is usually by reacting fluorenecarboxylic acid (9H-fluorene-9-carboxylic acid) with carbodiimide for amidation, and then performing a carbon-carbon bond formation reaction.
Regarding safety information, since this compound is used more in the laboratory, personal protective measures must be paid attention. Wear chemical protective gloves, safety goggles and protective clothing to avoid skin contact and inhalation. In addition, it must be operated in a well-ventilated laboratory environment to prevent the accumulation of harmful gases. It should be stored in a cool, dry place, away from flammable materials and oxidizing agents. In use or disposal, must comply with the relevant safety procedures and regulations.
Last Update:2024-04-09 21:04:16