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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Benzeneacetic acid, a-hydroxy-, hydrazide, (R)-

NNC(=O)[C@@H](c1ccccc1)O Request for Quotation
Chemical Name: Benzeneacetic acid, a-hydroxy-, hydrazide, (R)-
CAS Number: 84049-61-6
Product Number: AG003C93(AGN-PC-0UQ9N0)
Synonyms:
MDL No: MFCD21332895
Molecular Formula: C8H10N2O2
Molecular Weight: 166.1772

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
166.18g/mol
XLogP3:
-0.4
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
166.074g/mol
Monoisotopic Mass:
166.074g/mol
Topological Polar Surface Area:
75.4A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
155
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Derived from phenylacetohydrazide, (R)-2-Hydroxy-2-phenylacetohydrazide plays a crucial role in chemical synthesis as a versatile reagent. This compound serves as a building block in the preparation of various pharmacologically active molecules due to its unique structure and functionality. It is commonly employed in the synthesis of complex heterocycles and chiral compounds through asymmetric transformations. Additionally, (R)-2-Hydroxy-2-phenylacetohydrazide is utilized in the creation of diverse pharmaceutical intermediates and agrochemicals, showcasing its significance in organic chemistry research and development.