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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)-

(R)-(4-chlorophenyl)-cyclopropylmethanamine

NC(c1ccc(cc1)Cl)C1CC1 Request for Quotation
Chemical Name: (R)-(4-chlorophenyl)-cyclopropylmethanamine
CAS Number: 123312-22-1
Product Number: AG000KBR(AGN-PC-0KH8J2)
Synonyms:
MDL No: MFCD05191965
Molecular Formula: C10H12ClN
Molecular Weight: 181.6620

Identification/Properties

Computed Properties
Molecular Weight:
181.663g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
181.066g/mol
Monoisotopic Mass:
181.066g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
148
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:
1
Compound Is Canonicalized:
Yes

Safety Information

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(4-Chlorophenyl)-1-cyclopropylmethylamine is a versatile compound that finds application in various chemical synthesis processes. This compound is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals due to its unique structural properties and reactivity. Its cyclopropylmethylamine group serves as a valuable scaffold for introducing additional functional groups through various chemical reactions. Furthermore, the presence of the 4-chlorophenyl group in its structure allows for specific interactions with biological targets, making it a key intermediate in the development of novel drug molecules. In chemical synthesis, 1-(4-Chlorophenyl)-1-cyclopropylmethylamine serves as a valuable starting material for the creation of diverse compounds with desired pharmacological or agricultural properties. Its versatility and effectiveness make it a valuable tool in the hands of synthetic chemists striving to develop new and improved products for various industries.