1. Home
  2. 1-Propanol, 2-amino-3-[(phenylmethyl)thio]-, (2R)-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

1-Propanol, 2-amino-3-[(phenylmethyl)thio]-, (2R)-

OC[C@H](CSCc1ccccc1)N Request for Quotation
Chemical Name: 1-Propanol, 2-amino-3-[(phenylmethyl)thio]-, (2R)-
CAS Number: 85803-43-6
Product Number: AG003U7G(AGN-PC-0OK2UA)
Synonyms:
MDL No:
Molecular Formula: C10H15NOS
Molecular Weight: 197.2972

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
197.296g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
197.087g/mol
Monoisotopic Mass:
197.087g/mol
Topological Polar Surface Area:
71.6A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
126
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

GHS Pictogram:
N/A
Signal Word:
UN#:
N/A
Hazard Statements:
-
Precautionary Statements:
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


H-Cysteinol(Bzl), also known as benzyl cysteine, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure and reactivity make it a valuable tool in the creation of various organic compounds. H-Cysteinol(Bzl) is commonly used as a precursor in the synthesis of peptides, specifically in the formation of disulfide bonds between cysteine residues. This reagent acts as a protecting group for the thiol functionality of cysteine, facilitating controlled bond formation and manipulation during peptide synthesis. Additionally, H-Cysteinol(Bzl) is utilized in the production of complex organic molecules, pharmaceuticals, and bioactive compounds due to its ability to introduce cysteine residues in a chemoselective manner. Its compatibility with a wide range of chemical reactions makes it an essential tool for chemists working in the fields of organic synthesis and drug discovery.