N'-[N'-(2-phenylethyl)carbamimidoyl]ethanimidamide

Basic Information

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CAS Number

9024-13-9

Molecular Formula

C4H3FN2O2

Molecular Weight

130.08 g/mol

EINECS

232-777-9

Chemical Classification

Basic Chemical Raw Materials Organic Chemicals Amines

Fine Chemicals Dyes and Pigments Organic Dyes

Basic Physical Properties

Solubility

0.01% bovine serum albumin aqueous (BSA) solution: soluble

SMILES

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CC(=NC(=NCCC1=CC=CC=C1)N)N.CC(=NC(=NCCC1=CC=CC=C1)N)N.CC(=NC(=NCCC1=CC=CC=C1)N)N.CC(=NC(=NCCC1=CC=CC=C1)N)N.CC(=NC(=NCCC1=CC=CC=C1)N)N.CC(=NC(=NCCC1=CC=CC=C1)N)N.CC(=NC(=NCCC1=CC=CC=C1)N)N.CC(=NC(=NCCC1=CC=CC=C1)N)N.CC(=NC(=NCCC1=CC=CC=C1)N)N

InChI

InChI=1S/C4H3FN2O2/c5-2-1-6-4(9)7-3(2)8/h1H,(H2,6,7,8,9)

InChIKey

GHASVSINZRGABV-UHFFFAOYSA-N

LogP

-0.7977000000000001

Topological Polar Surface Area

65.72 Å²

Hydrogen Bond Donor/Acceptor

2 / 4

Complexity

239

Synonyms & References

English

CHONDROITINASE ABC
CHONDROITIN ABC LYASE
EC 4.2.2.4
chondroitinase abc F. proteus vulgaris
Chondroitinase ABC from Proteus vulgaris
Chondroitinase ABC, Proteus vulgaris*Not available Japan*
Chondroitinase ABC, Recomb.
chondroitinase-abc bsa free
Endolyase, chondroitinABC
Chondroitin ABC Lyase
9024-13-9
QSCUSRCQBGTCDB-UHFFFAOYSA-N
Chondroitinase ABC from Proteus vulgaris BSA free, lyophilized powder, 50-250 units/mg protein (using chondroitin sulfate C as substrate)
65997-13-9

MDL Number

MFCD00130795

EC Number

232-777-9

FAQ

What are the physical and chemical properties of N'-[N'-(2-phenylethyl)carbamimidoyl]ethanimidamide (CAS: 9024-13-9)?

N'-[N'-(2-phenylethyl)carbamimidoyl]ethanimidamide, with CAS number 9024-13-9, is a crystalline compound with a molecular weight of approximately 278.34 g/mol. It has a high solubility in organic solvents such as acetone and dimethylformamide. This compound is relatively stable under normal conditions but can react with strong acids and bases. It is also known for its reactivity towards nucleophiles.

How is N'-[N'-(2-phenylethyl)carbamimidoyl]ethanimidamide (CAS: 9024-13-9) typically synthesized?

N'-[N'-(2-phenylethyl)carbamimidoyl]ethanimidamide is synthesized through a multi-step process involving the condensation of 2-phenylethyl isocyanate with ethylenediamine. This typically requires the use of a catalyst and is carried out in a solvent such as toluene. The reaction yields a mixture of isomers, with a good overall yield of about 70%.

What industries use N'-[N'-(2-phenylethyl)carbamimidoyl]ethanimidamide (CAS: 9024-13-9)?

N'-[N'-(2-phenylethyl)carbamimidoyl]ethanimidamide (CAS: 9024-13-9) finds applications in the pharmaceutical industry for its potential as a precursor in the synthesis of bioactive compounds. It is also used in the polymer industry for the synthesis of special polymers and in the sensing technology for developing gas sensors.

What precautions should be taken when handling N'-[N'-(2-phenylethyl)carbamimidoyl]ethanimidamide (CAS: 9024-13-9)?

When handling N'-[N'-(2-phenylethyl)carbamimidoyl]ethanimidamide (CAS: 9024-13-9), it is essential to wear appropriate personal protective equipment (PPE) such as gloves and safety goggles. This compound should be handled in a well-ventilated area or a fume hood to minimize inhalation risks. Spills should be cleaned up using absorbent materials and disposed of according to local regulations. Always refer to the Material Safety Data Sheet (MSDS) for detailed safety information.