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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)-

4-HYDROXY-(2R,4R)-2-PYRROLIDINEMETHANOLHYDROCHLORIDE

OC[C@@H]1NC[C@@H](C1)O.Cl Request for Quotation
Chemical Name: 4-HYDROXY-(2R,4R)-2-PYRROLIDINEMETHANOLHYDROCHLORIDE
CAS Number: 1009335-36-7
Product Number: AG00038V(AGN-PC-0WAFIK)
Synonyms:
MDL No:
Molecular Formula: C5H12ClNO2
Molecular Weight: 153.6073

Identification/Properties

Properties
Storage:
Inert atmosphere;Room Temperature;
Computed Properties
Molecular Weight:
153.606g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
153.056g/mol
Monoisotopic Mass:
153.056g/mol
Topological Polar Surface Area:
52.5A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
76.8
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (3R,5R)-5-(Hydroxymethyl)pyrrolidin-3-ol hydrochloride plays a crucial role in chemical synthesis as a versatile building block. With its unique structure and reactivity, this compound is widely used as a key intermediate in the synthesis of various complex organic molecules. By incorporating (3R,5R)-5-(Hydroxymethyl)pyrrolidin-3-ol hydrochloride into chemical reactions, chemists can efficiently introduce functional groups and stereochemical elements into their target compounds. This compound's hydroxymethyl group and pyrrolidin-3-ol ring provide valuable points for further derivatization, enabling the creation of diverse molecular scaffolds. Additionally, the hydrochloride salt form enhances the compound's solubility and stability, facilitating its manipulation in synthetic processes. Overall, the (3R,5R)-5-(Hydroxymethyl)pyrrolidin-3-ol hydrochloride is a valuable tool for chemists seeking to design and construct intricate organic molecules through strategic chemical synthesis strategies.