Thiosulfuric acid O-sodium S-benzyl ester salt

Base Information

• Chemical Name: Thiosulfuric acid O-sodium S-benzyl ester salt
• CAS No.: 6313-36-6
• Molecular Formula: C7H8O3S2
• Molecular Weight: 226.253
• Mol file: 6313-36-6.mol

Synonyms:sodium S-benzyl sulfothioate;benzyl thiosulphate;Thioschwefelsaeure-S-benzylester,Natriumsalz;sodium benzyl thiosulfate;Thioschwefelsaeure-S-benzylester,Natrium-Verbindung;thiosulfuric acid S-benzyl ester,sodium-compound;Na-Benzylthiosulfat;Thiosulfuric acid S-benzyl O-sodium salt;Thiosulfuric acid O-sodium S-benzyl ester salt;

Chemical Property of Thiosulfuric acid O-sodium S-benzyl ester salt

Chemical Property:

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• PSA: 88.05000
• Density: 1.477g/cm³
• LogP: 2.80340

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Uses: Benzylthiosulfuric Acid Sodium Salt is an intermediate used in the synthesis of Benzyl Trisulfide (B316150), which is a secondary metabolite of Petiveria alliacea, on erythrocyte elasticity, relaxation time and membrane morphol. An antibacterial and antifungal agent.

Technology Process of Thiosulfuric acid O-sodium S-benzyl ester salt

There total 5 articles about Thiosulfuric acid O-sodium S-benzyl ester salt 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: 100.0%

benzyl bromide (100-39-0) → benzyl thiosulphate (6313-36-6)

Guidance literature:

With sodium thiosulfate; In water; toluene;

DOI:10.1016/0040-4039(94)88513-3

Reference yield: 93.0%

→ benzyl thiosulphate (6313-36-6)

Guidance literature:

With sodium thiosulfate; In ethanol; water; at 110 ℃; for 15h;

Reference yield: 76.0%

iodomethylbenzene (620-05-3) → benzyl thiosulphate (6313-36-6)

Guidance literature:

With sodium thiosulfate; benzyltrimethylammonium chloride; In methanol; water; Heating;

upstream raw materials:

benzyl chloride

benzyl bromide

iodomethylbenzene

Downstream raw materials:

acetyl benzyl disulfide

allyl(benzyl)sulfide

benzotriazolylmethyl phenylmethyl thioether

benzyl-(4-fluorophenyl)-sulfide

Refernces

• 1、 Tan, Wei,J?nsch, Niklas,?hlmann, Tina,Meyer-Almes, Franz-Josef,Jiang, Xuefeng. "Thiocarbonyl Surrogate via Combination of Potassium Sulfide and Chloroform for Dithiocarbamate Construction". supporting information. p. 7484 - 7488. Retrieved 2019/10/08.
• 2、 -. "Novel glucose-based brain-targeting prodrug with locking function". Paragraph 0027. . Retrieved 2016/10/10.