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1H-Pyrrolo[2,3-d]pyrimidine-5-carbonitrile, 4-[(triphenylmethyl)amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 141232-18-0 Structure
  • Basic information

    1. Product Name: 1H-Pyrrolo[2,3-d]pyrimidine-5-carbonitrile, 4-[(triphenylmethyl)amino]-
    2. Synonyms:
    3. CAS NO:141232-18-0
    4. Molecular Formula: C26H19N5
    5. Molecular Weight: 401.47
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 141232-18-0.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: 1H-Pyrrolo[2,3-d]pyrimidine-5-carbonitrile, 4-[(triphenylmethyl)amino]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Pyrrolo[2,3-d]pyrimidine-5-carbonitrile, 4-[(triphenylmethyl)amino]-(141232-18-0)
    11. EPA Substance Registry System: 1H-Pyrrolo[2,3-d]pyrimidine-5-carbonitrile, 4-[(triphenylmethyl)amino]-(141232-18-0)
  • 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: 141232-18-0(Hazardous Substances Data)

141232-18-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141232-18-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,2,3 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 141232-18:
(8*1)+(7*4)+(6*1)+(5*2)+(4*3)+(3*2)+(2*1)+(1*8)=80
80 % 10 = 0
So 141232-18-0 is a valid CAS Registry Number.

141232-18-0Relevant articles and documents

A SYNTHESIS AND AN X-RAY ANALYSIS OF 2'-C-, 3'-C- AND 5'-C-METHYLSANGIVAMYCINS

Murai, Yasushi,Shiroto, Hironori,Ishizaki, Tatsuya,Iimori, Takamasa,Kodama, Yoshio,et al.

, p. 391 - 404 (2007/10/02)

3'-C-, 5'(R)-C- and 5'(S)-C-Methylsangivamycins (3-5) were synthesized by the trimethylsilyl triflate mediated coupling reaction of the methyl substituted ribose derivatives (7), (9) and (10) with the base moiety (11) and the successive functional group m

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