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88001-11-0

C6H12NO3(1+) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 88001-11-0 Structure

  • Basic information

    1. Product Name: C6H12NO3(1+)
    2. Synonyms: C6H12NO3(1+)
    3. CAS NO:88001-11-0
    4. Molecular Formula:
    5. Molecular Weight: 146.166
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 88001-11-0.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: C6H12NO3(1+)(CAS DataBase Reference)
    10. NIST Chemistry Reference: C6H12NO3(1+)(88001-11-0)
    11. EPA Substance Registry System: C6H12NO3(1+)(88001-11-0)

  • 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: 88001-11-0(Hazardous Substances Data)

88001-11-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88001-11-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,0 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 88001-11:
(7*8)+(6*8)+(5*0)+(4*0)+(3*1)+(2*1)+(1*1)=110
110 % 10 = 0
So 88001-11-0 is a valid CAS Registry Number.

88001-11-0Downstream Products

88001-11-0Relevant articles and documents

IONIC HYDROGEN BOND. 4. INTRAMOLECULAR AND MULTIPLE BONDS. PROTONATION AND COMPLEXES OF AMIDES AND AMINO ACID DERIVATIVES.

Meot-Ner (Mautner)

, p. 278 - 283 (2007/10/02)

The paper examines the proton affinities and ionic hydrogen bonding of some amides and of the N-acetylated amino acid derivative CH//3CONHCH(CH//3)COOCH//3. The thermochemistry of these species can serve as a model for the energetics of protonated intermediates in acid hydrolysis of amides and the energetics of protonated amide groups in proteins.

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