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

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  • 30098-17-0 Structure
  • Basic information

    1. Product Name: Benzenepentanoic acid, 2,5-dimethyl-
    2. Synonyms:
    3. CAS NO:30098-17-0
    4. Molecular Formula: C13H18O2
    5. Molecular Weight: 206.285
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 30098-17-0.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: Benzenepentanoic acid, 2,5-dimethyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenepentanoic acid, 2,5-dimethyl-(30098-17-0)
    11. EPA Substance Registry System: Benzenepentanoic acid, 2,5-dimethyl-(30098-17-0)
  • 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: 30098-17-0(Hazardous Substances Data)

30098-17-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30098-17-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,0,9 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 30098-17:
(7*3)+(6*0)+(5*0)+(4*9)+(3*8)+(2*1)+(1*7)=90
90 % 10 = 0
So 30098-17-0 is a valid CAS Registry Number.

30098-17-0Downstream Products

30098-17-0Relevant articles and documents

On the conformation of 8-membered ring heterocycles - Dynamic and static conformational analysis of acylated hexahydrobenzazocines

Hassner, Alfred,Amit, Boaz,Marks, Vered,Gottlieb, Hugo E.

, p. 1256 - 1261 (2006)

A high-field NMR analysis of several acylated hexahydrobenzazocines indicates that, surprisingly, ring methylene groups are typically diastereotopic at room temperature, as the barriers for the process of enantiomerization of the eight - membered ring are

Alternative procedure for the synthesis of (+)-tavacpallescencine precursor

Banerjee,Vera,Laya

, p. 855 - 857 (2002)

A conversion of dimethylbenzo[d]suberone prepared from 5-chlorovaleric acid into butenolide, a precursor of tavacpallescencine, was described.

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