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60725-23-7

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60725-23-7 Usage

Uses

thiadiazole pharmaceutical intermediate

Check Digit Verification of cas no

The CAS Registry Mumber 60725-23-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,2 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 60725-23:
(7*6)+(6*0)+(5*7)+(4*2)+(3*5)+(2*2)+(1*3)=107
107 % 10 = 7
So 60725-23-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H6N2O2S3/c1-2(3(8)9)11-5-7-6-4(10)12-5/h2H,1H3,(H,6,10)(H,8,9)

60725-23-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2-sulfanylidene-3H-1,3,4-thiadiazol-5-yl)sulfanyl]propanoic acid

1.2 Other means of identification

Product number -
Other names 2-(5-Mercapto-1,3,4-thiadiazol-2-ylthio)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:60725-23-7 SDS

60725-23-7Downstream Products

60725-23-7Relevant articles and documents

Synthesis of novel 2-substituted thiadiazole derivatives

Xue, Shouqing,Ma, Yuanzhong,Li, Weinan

, p. 383 - 387 (2018/06/06)

Seven mild, efficient and novel inhibitors were obtained in good to excellent yield by addition of Thiadiazole derivatives with an acidsmolecular sieve system at moderate temperature (50C). The structures of the prepared compounds are characterized by IR and1HNMR Spectroscopy, and the catalyst can be recovered by filtration and reused several times. The resulted showed that the process was then applied to [1, 3, 4] thiadiazde derivatives using 0.75 g of Catalyst for acids and performing the reactions at 50 °C for 1 hour with sulfuric acid as solvent (15mL, 70%). We have shown for the first time that a heterogeneous catalyst, namely commercially available AlPO45 and SBA15 molecular sieve, can be successfully and efficiently utilized for the highly selective synthesis of 3. Moreover, the use of sulfuric acid as solvent, the high atom economy, and the possibility of recycling the catalyst for several runs, make this approach practical and environmentally acceptable.

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