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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)-

methyl 2-amino-2-(3,4-dichlorophenyl)acetate;hydrochloride

COC(=O)C(c1ccc(c(c1)Cl)Cl)N.Cl Request for Quotation
Chemical Name: methyl 2-amino-2-(3,4-dichlorophenyl)acetate;hydrochloride
CAS Number: 1078611-21-8
Product Number: AG003RMC(AGN-PC-04HB4C)
Synonyms:
MDL No: MFCD04115512
Molecular Formula: C9H10Cl3NO2
Molecular Weight: 270.5402

Identification/Properties

Properties
Storage:
2-8℃;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
270.534g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
268.978g/mol
Monoisotopic Mass:
268.978g/mol
Topological Polar Surface Area:
52.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
213
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 2-amino-2-(3,4-dichlorophenyl)acetate hydrochloride, known for its versatile chemical properties, is widely recognized for its utility in chemical synthesis. This compound serves as a key intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and reactivity make it a valuable building block for creating complex molecules through organic synthesis. In particular, Methyl 2-amino-2-(3,4-dichlorophenyl)acetate hydrochloride is prized for its ability to participate in diverse transformations, such as acylation reactions, nucleophilic substitutions, and catalytic processes. As a result, it plays a crucial role in the development of new drugs, pesticides, and materials with enhanced performance characteristics. Its strategic use in chemical synthesis underscores its significance in advancing modern science and technology.