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(1S,2S)-(+)-2-AMINO-1-[4-(METHYLTHIO)PHENYL]-1,3-PROPANEDIOL
  • Chemical Name: (1S,2S)-(+)-2-AMINO-1-[4-(METHYLTHIO)PHENYL]-1,3-PROPANEDIOL
  • CAS No.: 16854-32-3

Quality products?make an important contribution to long-term revenue and profitability. Excellent chemical plant bulk supply (1S,2S)-(+)-2-AMINO-1-[4-(METHYLTHIO)PHENYL]-1,3-PROPANEDIOL 16854-32-3

1.What is the (1S,2S)-(+)-2-AMINO-1-[4-(METHYLTHIO)PHENYL]-1,3-PROPANEDIOL ?

(1S,2S)-(+)-Thiomicamine can be used:As a starting material in the synthesis of 3,4-dihydroisoquinolinium salts, which are employed as promoters in asymmetric epoxidation and oxidation?reactions.As a starting material in the synthesis of an α-amino acid named (3R,4R)-4-phenyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid, which is used to prepare modified peptides of biological importance.As a chiral base in the resolution of an angiotensin II type 2 receptor [AT2R] antagonist named EMA401.

(1<i>RS</i>,2<i>RS</i>)-2-acetylamino-1-(4-methylsulfanyl-phenyl)-propane-1,3-diol
23150-33-6,23150-34-7,27348-35-2,27348-43-2,27348-46-5,60658-37-9

(1RS ,2RS )-2-acetylamino-1-(4-methylsulfanyl-phenyl)-propane-1,3-diol

(1<i>RS</i>,2<i>RS</i>)-2-amino-1-(4-methylsulfanyl-phenyl)-propane-1,3-diol
14172-52-2,16854-32-3,23150-35-8,27348-36-3,27348-47-6,27348-48-7,36624-58-5

(1RS ,2RS )-2-amino-1-(4-methylsulfanyl-phenyl)-propane-1,3-diol

Conditions
Conditions Yield
With hydrogenchloride;
<i>N</i>-[1-hydroxymethyl-2-(4-methylsulfanyl-phenyl)-2-oxo-ethyl]-acetamide
38423-42-6

N -[1-hydroxymethyl-2-(4-methylsulfanyl-phenyl)-2-oxo-ethyl]-acetamide

(1<i>RS</i>,2<i>RS</i>)-2-amino-1-(4-methylsulfanyl-phenyl)-propane-1,3-diol
14172-52-2,16854-32-3,23150-35-8,27348-36-3,27348-47-6,27348-48-7,36624-58-5

(1RS ,2RS )-2-amino-1-(4-methylsulfanyl-phenyl)-propane-1,3-diol

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1: aluminium isopropylate; isopropyl alcohol
2: aqueous HCl
With hydrogenchloride; aluminum isopropoxide; isopropyl alcohol;

2.What is the CAS number for (1S,2S)-(+)-2-AMINO-1-[4-(METHYLTHIO)PHENYL]-1,3-PROPANEDIOL ?

The CAS number of (1S,2S)-(+)-2-AMINO-1-[4-(METHYLTHIO)PHENYL]-1,3-PROPANEDIOL is 16854-32-3.

More information of (1S,2S)-(+)-2-AMINO-1-[4-(METHYLTHIO)PHENYL]-1,3-PROPANEDIOL 16854-32-3 are:

CAS?Number

16854-32-3

Density

1.25g/cm3

Melting Point

151-154 °C(lit.)

Boiling Point

428.2°Cat760mmHg

Flash Point

212.8°C

Vapor Pressure

4.29E-08mmHg at 25°C

Refractive Index

1.624

HS CODE

2930909090

PSA

91.78000

LogP

1.46180

Pka

11.75±0.45(Predicted)

3.What are another words for (1S,2S)-(+)-2-AMINO-1-[4-(METHYLTHIO)PHENYL]-1,3-PROPANEDIOL ?

Synonyms?for?(1S,2S)-(+)-2-AMINO-1-[4-(METHYLTHIO)PHENYL]-1,3-PROPANEDIOL 16854-32-3:1,3-Propanediol,2-amino-1-[4-(methylthio)phenyl]-, [S-(R*,R*)]-; 1,3-Propanediol,2-amino-1-[p-(methylthio)phenyl]-, threo-(+)- (8CI); (+)-Thiomicamine;(1S*,2S*)-(+)-Thiomicamine;(1S,2S)-2-Amino-1-(4-methylsulfanylphenyl)-1,3-propanediol;L-threo-(+)-2-Amino-1-(4-methylthiophenyl)-1,3-propanediol; Thiomicamine

4.What is the molecular formula of (1S,2S)-(+)-2-AMINO-1-[4-(METHYLTHIO)PHENYL]-1,3-PROPANEDIOL?

The chemical formula of ?(1S,2S)-(+)-2-AMINO-1-[4-(METHYLTHIO)PHENYL]-1,3-PROPANEDIOL is?C10H15 N O2 S which containing 10 Carbon atoms,15 Hydrogen atoms,1 Nitrogen atoms,2 Oxygen atoms and 1 Sulfur atoms,and the molecular weight of??(1S,2S)-(+)-2-AMINO-1-[4-(METHYLTHIO)PHENYL]-1,3-PROPANEDIOL?is 213.301.

5.What is (1S,2S)-(+)-2-AMINO-1-[4-(METHYLTHIO)PHENYL]-1,3-PROPANEDIOL (16854-32-3) used for?

(1S,2S)-(+)-2-AMINO-1-[4-(METHYLTHIO)PHENYL]-1,3-PROPANEDIOL, also known as (1S,2S)-(+)-Thiomicamine, is an organic compound with a unique structure that features a chiral center and a methylthio group. It is characterized by its optical activity and is a valuable building block in the synthesis of various biologically active molecules.

InChI:InChI=1/C10H15NO2S/c1-14-8-4-2-7(3-5-8)10(13)9(11)6-12/h2-5,9-10,12-13H,6,11H2,1H3/t9-,10-/m0/s1

Relevant articles related to (1S,2S)-(+)-2-AMINO-1-[4-(METHYLTHIO)PHENYL]-1,3-PROPANEDIOL:

Article

Source

Reversed-phase liquid chromatographic separation of enantiomeric and diastereomeric bases related to chloramphenicol and thiamphenicol.

Gal,Meyer-Lehnert

, p. 1062 - 1065 (2007/10/02)

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