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Benzoic acid, 2-amino-5-butyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 18331-73-2 Structure
  • Basic information

    1. Product Name: Benzoic acid, 2-amino-5-butyl-
    2. Synonyms:
    3. CAS NO:18331-73-2
    4. Molecular Formula: C11H15NO2
    5. Molecular Weight: 193.246
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 18331-73-2.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: Benzoic acid, 2-amino-5-butyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid, 2-amino-5-butyl-(18331-73-2)
    11. EPA Substance Registry System: Benzoic acid, 2-amino-5-butyl-(18331-73-2)
  • 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: 18331-73-2(Hazardous Substances Data)

18331-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18331-73-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,3 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 18331-73:
(7*1)+(6*8)+(5*3)+(4*3)+(3*1)+(2*7)+(1*3)=102
102 % 10 = 2
So 18331-73-2 is a valid CAS Registry Number.

18331-73-2Relevant articles and documents

THERAPEUTICALLY ACTIVE COMPOUNDS FOR USE IN THE TREATMENT OF CANCER CHARACTERIZED AS HAVING AN IDH MUTATION

-

Page/Page column 105, (2011/06/26)

Compounds and compositions comprising compounds useful in the treatment of cancer are described herein. The compounds and compositions can be used to modulate an isocitrate dehydrogenase (IDH) mutant (e.g., IDHIm or IDH2m) having alpha hydroxyl neoactivity

Organic field-effect transistors based on solution-processible dibenzotetrathiafulvalene derivatives

Yoshino, Takamasa,Shibata, Koji,Wada, Hiroshi,Bando, Yoshimasa,Ishikawa, Ken,Takezoe, Hideo,Mori, Takehiko

supporting information; experimental part, p. 200 - 201 (2010/03/02)

Organic field-effect transistors based on alkyl-substituted dibenzotetrathiafulvalenes (DBTTF) are fabricated by solution process. The molecules with butyl or longer alkyl groups are standing perpendicular to the substrates in the thin films, and the tran

LIQUID-CRYSTAL 4H-3,1-BENZOXAZIN-4-ONES

Bolotin, B. M.,Zeryukina, L. S.,Safina, R. U.,Egorkin, V. V.,Kuliev, R. I.

, p. 996 - 998 (2007/10/02)

2,6-Disubstituted 4H-3,1-benzoxazin-4-ones that have mesogenic properties were synthesized by the reaction of 5-substituted anthranilic acid with aroyl chlorides in pyridine.The introduction of a 4H-3,1-benzoxazin-4-one fragment increases the absolute val

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