CAS 5331-43-1
:Phenylmethyl hydrazinecarboxylate
Description:
Phenylmethyl hydrazinecarboxylate, with the CAS number 5331-43-1, is an organic compound characterized by its hydrazine and carboxylate functional groups. It typically appears as a colorless to pale yellow liquid or solid, depending on its purity and specific form. This compound is known for its reactivity, particularly in the presence of electrophiles, due to the nucleophilic nature of the hydrazine moiety. It can participate in various chemical reactions, including condensation and substitution reactions, making it useful in synthetic organic chemistry. Additionally, phenylmethyl hydrazinecarboxylate may exhibit biological activity, which can be of interest in pharmaceutical research. Its solubility in organic solvents and moderate stability under standard conditions are notable characteristics, although it should be handled with care due to potential toxicity associated with hydrazine derivatives. Proper safety protocols should be followed when working with this compound, including the use of personal protective equipment and working in a well-ventilated area.
Formula:C8H10N2O2
InChI:InChI=1S/C8H10N2O2/c9-10-8(11)12-6-7-4-2-1-3-5-7/h1-5H,6,9H2,(H,10,11)
InChI key:InChIKey=RXUBZLMIGSAPEJ-UHFFFAOYSA-N
SMILES:C(OC(NN)=O)C1=CC=CC=C1
Synonyms:- (+)-Biotin N-hydroxysuccinimide ester
- Benzyl hydrazinecarboxylate
- Benzyl hydrazinocarboxylate
- Benzyloxycarbonyl hydrazide
- Carbazic acid, benzyl ester
- Carbobenzoxyhydrazide
- Carbobenzyloxyhydrazine
- Hydrazincarboxylic acid benzyl ester
- Hydrazinecarboxylic Acid Benzyl Ester
- Hydrazinecarboxylic acid, phenylmethyl ester
- N-(Benzyloxycarbonyl)hydrazine
- NSC 2287
- Phenylmethyl hydrazinecarboxylate
- [(Benzyloxy)carbonyl]hydrazine
- See more synonyms
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Found 7 products.
Benzyl Carbazate
CAS:Formula:C8H10N2O2Purity:>98.0%(T)Color and Shape:White to Orange to Green powder to crystalMolecular weight:166.18Benzyl carbazate, 98+%
CAS:<p>Benzyl carbazate is used as a reagent for preparation of benzyloxycarbonyl (Z, Cbz) hydrazides of carboxylic acids, particularly N-protected amino acids. Subsequent hydrogenolysis gives the hydrazide which can be converted to the azide for coupling with a further amino acid residue by the azide meth</p>Formula:C8H10N2O2Purity:98+%Color and Shape:White to pale yellow, Crystalline powder or flakesMolecular weight:166.18Benzyl hydrazinecarboxylate
CAS:Formula:C8H10N2O2Purity:95%Color and Shape:SolidMolecular weight:166.1772Hydrazine, N-CBZ protected
CAS:<p>Hydrazine, N-CBZ protected</p>Formula:C8H10N2O2Purity:≥95%Color and Shape: white crystalline solidMolecular weight:166.18g/molN-α-Z-hydrazide
CAS:<p>N-alpha-Z-hydrazide is a cyclic peptide that is active against bacterial infections, including infectious diseases and autoimmune diseases. It has been shown to be effective against mouse models of inflammatory bowel disease, multiple sclerosis, and arthritis. The compound is also used as an experimental model for studying the effects of drugs on biological systems. N-alpha-Z-hydrazide binds to the Mcl-1 protein in a coordinated geometry that prevents its interaction with other proteins. This binding leads to cell death by preventing the release of cytochrome C from mitochondria and reducing mitochondrial membrane potential. N-alpha-Z-hydrazide has demonstrated antiinflammatory activity in mice which may be due to its inhibition of prostaglandin synthesis.</p>Formula:C8H10N2O2Purity:Min. 95%Color and Shape:PowderMolecular weight:166.18 g/molBenzyl carbazate
CAS:Formula:C8H10N2O2Purity:95%Color and Shape:Solid, Crystalline Powder or FlakesMolecular weight:166.18Benzyl Carbazate
CAS:Controlled Product<p>Applications Benzyl Carbazate has been shown to prevent the occurrence of oligonucleosome-sized DNA fragmentation in the cell-free system.<br>References Sane, A.-T. et al.: Cancer Res., 58, 3066 (1998);<br></p>Formula:C8H10N2O2Color and Shape:NeatMolecular weight:166.18






