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51542-42-8

methyl 4-(5-amino-1,3,4-thiadiazol-2-yl)benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 51542-42-8 Structure

  • Basic information

    1. Product Name: methyl 4-(5-amino-1,3,4-thiadiazol-2-yl)benzoate
    2. Synonyms: methyl 4-(5-amino-1,3,4-thiadiazol-2-yl)benzoate
    3. CAS NO:51542-42-8
    4. Molecular Formula: C10H9N3O2S
    5. Molecular Weight: 235.26236
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 51542-42-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 427.1±47.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.377±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 2.18±0.10(Predicted)
    10. CAS DataBase Reference: methyl 4-(5-amino-1,3,4-thiadiazol-2-yl)benzoate(CAS DataBase Reference)
    11. NIST Chemistry Reference: methyl 4-(5-amino-1,3,4-thiadiazol-2-yl)benzoate(51542-42-8)
    12. EPA Substance Registry System: methyl 4-(5-amino-1,3,4-thiadiazol-2-yl)benzoate(51542-42-8)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 51542-42-8(Hazardous Substances Data)

51542-42-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51542-42-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,4 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 51542-42:
(7*5)+(6*1)+(5*5)+(4*4)+(3*2)+(2*4)+(1*2)=98
98 % 10 = 8
So 51542-42-8 is a valid CAS Registry Number.

51542-42-8Relevant articles and documents

Efficient Synthesis of Five Types of Heterocyclic Compounds via Intramolecular Elimination Using Ultrasound-Static Heating Technique

Jiang, Hongfei,Dong, Xueyang,Jin, Xin,Zhu, Danyang,Yin, Ruijuan,Yu, Rilei,Wan, Shengbiao,Zhang, Lijuan,Jiang, Tao

supporting information, p. 2009 - 2013 (2018/07/31)

An experimental technique, ultrasound-static heating, has been developed for the efficient synthesis of heterocyclic compounds. The technique involves ultrasonic irradiation and static heating processes. First, the ultrasonic irradiation process is performed to form an intermediate of the heterocyclic compound under mild conditions and the subsequent static heating process (heating the intermediate under solvent-free conditions without stirring) produces the target heterocyclic compounds via intramolecular elimination.

Structure-based design of novel potent protein kinase CK2 (CK2) inhibitors with phenyl-azole scaffolds

Hou, Zengye,Nakanishi, Isao,Kinoshita, Takayoshi,Takei, Yoshinori,Yasue, Misato,Misu, Ryosuke,Suzuki, Yamato,Nakamura, Shinya,Kure, Tatsuhide,Ohno, Hiroaki,Murata, Katsumi,Kitaura, Kazuo,Hirasawa, Akira,Tsujimoto, Gozoh,Oishi, Shinya,Fujii, Nobutaka

, p. 2899 - 2903 (2012/06/01)

Protein kinase CK2 (CK2) is a ubiquitous serine/threonine protein kinase for hundreds of endogenous substrates. CK2 has been considered to be involved in many diseases, including cancers. Herein we report the discovery of a novel ATP-competitive CK2 inhibitor. Virtual screening of a compound library led to the identification of a hit 2-phenyl-1,3,4-thiadiazole compound. Subsequent structural optimization resulted in the identification of a promising 4-(thiazol-5-yl)benzoic acid derivative.

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