2-(L-RHAMNO-TETRAHYDROXYPENTYL)-4(R)-1,3-THIAZOLIDINE-4-CARBOXYLIC ACID

Base Information

• Chemical Name: 2-(L-RHAMNO-TETRAHYDROXYPENTYL)-4(R)-1,3-THIAZOLIDINE-4-CARBOXYLIC ACID
• CAS No.: 115184-32-2
• Molecular Formula: C₉H₁₇NO₆S
• Molecular Weight: 267.303
• Mol file: 115184-32-2.mol

Synonyms:2-(L-RHAMNO-TETRAHYDROXYPENTYL)-4(R)-1,3-THIAZOLIDINE-4-CARBOXYLIC ACID

Chemical Property of 2-(L-RHAMNO-TETRAHYDROXYPENTYL)-4(R)-1,3-THIAZOLIDINE-4-CARBOXYLIC ACID

Chemical Property:

• Boiling Point: 633.0±55.0 °C(Predicted)
• PKA: 1.97±0.40(Predicted)
• PSA: 155.55000
• Density: 1.547±0.06 g/cm3(Predicted)
• LogP: -2.10560

Purity/Quality:

98%min ^*data from raw suppliers

2-(L-Rhamno-tetrahydroxypentyl)-4(R)-1-3-thiazolidine-4-carboxylicacid ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 2-(L-RHAMNO-TETRAHYDROXYPENTYL)-4(R)-1,3-THIAZOLIDINE-4-CARBOXYLIC ACID

There total 6 articles about 2-(L-RHAMNO-TETRAHYDROXYPENTYL)-4(R)-1,3-THIAZOLIDINE-4-CARBOXYLIC ACID which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

kaempferol 3-O-β-D-xylopyranosyl-(1→2)-α-L-rhamnopyranosyl-7-O-α-L-rhamnopyranoside (124704-85-4) + L-cysteine methyl ester hydrochloride (18598-63-5) → L-cysteine-L-rhamnose (30080-13-8,30086-01-2,115184-31-1,115184-32-2,144664-40-4) + 2(RS)-D-xylo-(1',2',3',4'-tetrahydroxybutyl)thiazolidine-4(R)-carboxylic acid (329323-20-8)

Guidance literature:

kaempferol 3-O-β-D-xylopyranosyl-(1→2)-α-L-rhamnopyranosyl-7-O-α-L-rhamnopyranoside; With hydrogenchloride; In water; at 80 ℃; for 4h;

L-cysteine methyl ester hydrochloride; With pyridine; at 60 ℃; for 1h;

DOI:10.1016/j.carres.2012.10.008

Reference yield:

kaempferol 3-O-β-D-xylopyranosyl-(1→2)-α-L-arabinofuranosyl-7-O-α-L-rhamnopyranoside (1415248-05-3) + L-cysteine methyl ester hydrochloride (18598-63-5) → L-cysteine-L-rhamnose (30080-13-8,30086-01-2,115184-31-1,115184-32-2,144664-40-4) + 2(RS)-D-xylo-(1',2',3',4'-tetrahydroxybutyl)thiazolidine-4(R)-carboxylic acid (329323-20-8) + (4R)-2-(L-arabino-1,2,3,4-Tetrahydroxybutyl)-4-thiazolidincarbonsaeure (280108-19-2)

Guidance literature:

kaempferol 3-O-β-D-xylopyranosyl-(1→2)-α-L-arabinofuranosyl-7-O-α-L-rhamnopyranoside; With hydrogenchloride; In water; at 80 ℃; for 4h;

L-cysteine methyl ester hydrochloride; With pyridine; at 60 ℃; for 1h;

DOI:10.1016/j.carres.2012.10.008

Reference yield:

L-Rhamnose (3615-41-6,478518-52-4) + l-cysteine hydrochloride (52-89-1) → L-cysteine-L-rhamnose (30080-13-8,30086-01-2,115184-31-1,115184-32-2,144664-40-4)

Guidance literature:

With pyridine; In water; for 12h;

DOI:10.1039/DT9900003155

upstream raw materials:

L-Cysteine

L-Rhamnose

l-cysteine hydrochloride

kaempferol 3-O-β-D-xylopyranosyl-(1→2)-α-L-rhamnopyranosyl-7-O-α-L-rhamnopyranoside

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