4-Nitrobenzyl (5R)-6-[(1R)-1-hydroxyethyl]-3,7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate

Basic Information

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CAS Number

9002-83-9

Molecular Formula

C16H16N2O7

Molecular Weight

116.47 g/mol

Chemical Classification

Fine Chemicals Specialty Chemicals UV Stabilizers

Electronic Chemicals Semiconductor Materials Etchants

Water Treatment Chemicals Disinfectants Chlorine Compounds

Basic Physical Properties

Melting Point

210℃

Boiling Point

°Cat760mmHg

Density

1 g/mL at 25 °C

SMILES

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C(=C(F)Cl)(F)F

InChI

InChI=1S/C16H16N2O7/c1-8(19)13-11-6-12(20)14(17(11)15(13)21)16(22)25-7-9-2-4-10(5-3-9)18(23)24/h2-5,8,11,13-14,19H,6-7H2,1H3/t8-,11-,13?,14?/m1/s1

InChIKey

YBIDYTOJOXKBLO-KRZNCCGCSA-N

LogP

2.2603

Topological Polar Surface Area

0.0 Å²

Hydrogen Bond Donor/Acceptor

0 / 0

Complexity

72.9

Synonyms & References

English

Trifluorchlorethylen
AF215GW34G
1-CHLORO-1,2,2-TRIFLUORO-ETHENE
C2F3Cl
2-Chloro-1,1,2-trifluoroethylene
Halocarbon oil 0.8
9002-83-9
1-chloranyl-1,2,2-tris(fluoranyl)ethene
CFE
CFC-1113
Trifluorovinyl chloride
79-38-9
NS00011105
Trifluorchlorethylen [Czech]
CF2=CFCl
Trifluoromonochloroethylene
CHLOROTRIFLUOROETHYLENE
Chlorotrifluoroethene
chlorotrifluorethylene
Fluoroplast 3
Monochlorotrifluoroethylene
1-Chloro-1,2,2-trifluoroethene
chlorotrifluoroetylene
1-Chloro-1,2,2-trifluoroethylene
Kel-F
CTFE
Chlorotrifluoroethylene, 98%
Ethylene, trifluorochloro-
HaloVac 190 oil
Daiflon
trifluoro-chloroethylene

MDL Number

MFCD00147324

FAQ

What are the physical and chemical properties of 4-Nitrobenzyl (5R)-6-[(1R)-1-hydroxyethyl]-3,7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate (CAS: 9002-83-9)?

4-Nitrobenzyl (5R)-6-[(1R)-1-hydroxyethyl]-3,7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate is a crystalline compound with a molecular weight of approximately 413.11 g/mol. It is moderately soluble in organic solvents like methanol and ethanol and slightly soluble in water. The compound is known for its reactivity towards nucleophiles, particularly due to the presence of carboxylic acid and hydroxyethyl functionalities.

How is 4-Nitrobenzyl (5R)-6-[(1R)-1-hydroxyethyl]-3,7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate (CAS: 9002-83-9) typically synthesized?

4-Nitrobenzyl (5R)-6-[(1R)-1-hydroxyethyl]-3,7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate is synthesized through a multi-step process involving nitration of the benzyl group followed by a ring-opening reaction to introduce the azabicyclo[3.2.0]heptane structure. Common reactions include use of nitric acid, acetic anhydride, and other reagents. The product typically has a yield of 70-80%.

What industries use 4-Nitrobenzyl (5R)-6-[(1R)-1-hydroxyethyl]-3,7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate (CAS: 9002-83-9)?

4-Nitrobenzyl (5R)-6-[(1R)-1-hydroxyethyl]-3,7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate is primarily used in the pharmaceutical industry for the development of drug molecules and in the polymer industry as a monomer. It also finds applications in sensor technology and semiconductor manufacturing due to its functional groups.

What precautions should be taken when handling 4-Nitrobenzyl (5R)-6-[(1R)-1-hydroxyethyl]-3,7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate (CAS: 9002-83-9)?

When handling 4-Nitrobenzyl (5R)-6-[(1R)-1-hydroxyethyl]-3,7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate, it is important to wear appropriate personal protective equipment (PPE), including gloves, goggles, and a lab coat. Work should be conducted in a fume hood to minimize inhalation risks. Spills should be cleaned up using appropriate absorbents, and the material safety data sheet (MSDS) or safety data sheet (SDS) should be consulted for detailed instructions.