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CAS

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790230-25-0

2'-benzyl 2-tert-butyl 4-methyl 4'-nitrobiphenyl-2,2',4-tricarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 790230-25-0 Structure

  • Basic information

    1. Product Name: 2'-benzyl 2-tert-butyl 4-methyl 4'-nitrobiphenyl-2,2',4-tricarboxylate
    2. Synonyms: 2'-benzyl 2-tert-butyl 4-methyl 4'-nitrobiphenyl-2,2',4-tricarboxylate
    3. CAS NO:790230-25-0
    4. Molecular Formula:
    5. Molecular Weight: 491.497
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 790230-25-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2'-benzyl 2-tert-butyl 4-methyl 4'-nitrobiphenyl-2,2',4-tricarboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2'-benzyl 2-tert-butyl 4-methyl 4'-nitrobiphenyl-2,2',4-tricarboxylate(790230-25-0)
    11. EPA Substance Registry System: 2'-benzyl 2-tert-butyl 4-methyl 4'-nitrobiphenyl-2,2',4-tricarboxylate(790230-25-0)

  • 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: 790230-25-0(Hazardous Substances Data)

790230-25-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 790230-25-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,0,2,3 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 790230-25:
(8*7)+(7*9)+(6*0)+(5*2)+(4*3)+(3*0)+(2*2)+(1*5)=150
150 % 10 = 0
So 790230-25-0 is a valid CAS Registry Number.

790230-25-0Relevant articles and documents

One-pot synthetic procedure for 2,2′-disubstituted biaryls via the Suzuki coupling reaction of aryl triflates in a biphasic solvent system

Miura, Masanori,Koike, Takanori,Ishihara, Tsukasa,Hirayama, Fukushi,Sakamoto, Shuichi,Okada, Minoru,Ohta, Mitsuaki,Tsukamoto, Shin-Ichi

, p. 3809 - 3820 (2006)

A one-pot synthetic procedure for 2,2′-disubstituted biaryls was developed via a Suzuki cross-coupling reaction of aryl triflates in a biphasic solvent system. The effects of various bases and solvents were investigated. Results showed that the Na2/

Design, synthesis and biological activity of selective and orally available TF/FVIIa complex inhibitors containing non-amidine P1 ligands

Miura, Masanori,Seki, Norio,Koike, Takanori,Ishihara, Tsukasa,Niimi, Tatsuya,Hirayama, Fukushi,Shigenaga, Takeshi,Sakai-Moritani, Yumiko,Tagawa, Ayako,Kawasaki, Tomihisa,Sakamoto, Shuichi,Okada, Minoru,Ohta, Mitsuaki,Tsukamoto, Shin-ichi

, p. 160 - 173 (2007/10/03)

We found the novel selective and orally available non-amidine TF/FVIIa complex inhibitor 21e, 4-({[(1S)-(aminocarbonyl)-3-methylbutyl]amino}carbonyl)-2′-({[4- (aminomethyl)phenyl]amino}carbonyl)-4′-(methylamino)biphenyl-2- carboxylic acid. The derivatives

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