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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)-

3-Thiomorpholinecarboxylic acid, hydrochloride

OC(=O)C1CSCCN1.Cl Request for Quotation
Chemical Name: 3-Thiomorpholinecarboxylic acid, hydrochloride
CAS Number: 96612-95-2
Product Number: AG005TLQ(AGN-PC-079VAV)
Synonyms:
MDL No:
Molecular Formula: C5H10ClNO2S
Molecular Weight: 183.6564

Identification/Properties

Properties
BP:
356.1°C at 760 mmHg
Storage:
2-8℃;Light sensitive;
Form:
Solid
Computed Properties
Molecular Weight:
183.65g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
183.012g/mol
Monoisotopic Mass:
183.012g/mol
Topological Polar Surface Area:
74.6A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
118
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Thiomorpholine-3-carboxylic acid hydrochloride is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. This compound serves as a key building block in the creation of various organic molecules, particularly in the pharmaceutical and agrochemical industries.In chemical synthesis, Thiomorpholine-3-carboxylic acid hydrochloride acts as a valuable intermediate for the preparation of complex organic compounds. Its functional groups and molecular structure enable it to undergo a variety of synthetic transformations, including substitution reactions, condensation reactions, and cycloadditions. By incorporating Thiomorpholine-3-carboxylic acid hydrochloride into the synthesis of target molecules, chemists can introduce the thiomorpholine moiety into the final product, imparting specific chemical and biological properties.Furthermore, Thiomorpholine-3-carboxylic acid hydrochloride offers the benefit of enhancing the overall efficiency of chemical reactions by facilitating desired bonding patterns and structural arrangements. Its use in chemical synthesis not only enables the creation of new molecules with tailored properties but also streamlines synthetic pathways, leading to improved yields and reduced waste.Overall, Thiomorpholine-3-carboxylic acid hydrochloride plays a crucial role in the realm of chemical synthesis, serving as a valuable tool for the construction of diverse organic compounds with applications spanning various industries.