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133089-16-4

6-Acetylamino-2-[(Z)-benzyloxyimino]-hexanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133089-16-4 Structure

  • Basic information

    1. Product Name: 6-Acetylamino-2-[(Z)-benzyloxyimino]-hexanoic acid
    2. Synonyms:
    3. CAS NO:133089-16-4
    4. Molecular Formula:
    5. Molecular Weight: 292.335
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133089-16-4.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: 6-Acetylamino-2-[(Z)-benzyloxyimino]-hexanoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-Acetylamino-2-[(Z)-benzyloxyimino]-hexanoic acid(133089-16-4)
    11. EPA Substance Registry System: 6-Acetylamino-2-[(Z)-benzyloxyimino]-hexanoic acid(133089-16-4)

  • 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: 133089-16-4(Hazardous Substances Data)

133089-16-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133089-16-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,0,8 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 133089-16:
(8*1)+(7*3)+(6*3)+(5*0)+(4*8)+(3*9)+(2*1)+(1*6)=114
114 % 10 = 4
So 133089-16-4 is a valid CAS Registry Number.

133089-16-4Relevant articles and documents

Lysine 2,3-Aminomutase: Role of S-Adenosyl-L-methionine in the Mechanism. Demonstration of Tritium Transfer from (2RS,3RS)-Lysine to S-Adenosyl-L-methionine

Kilgore, James L.,Aberhart, D. John

, p. 79 - 84 (2007/10/02)

(2RS,3RS)-Lysine has been synthesized, and incubated with lysine 2,3-aminomutase in the presence of S-adenosyl-L-methionine (SAM).After incubation, the SAM was converted, by heating, into methylthioadenosine (MTA).The latter contained ca. 1-6percent of the incubated tritium, consistent with an exchange of SAM hydrogens (probably at C-5') with the 3-pro-R hydrogen of lysine.The results support a mechanism for lysine 2,3-aminomutase in which SAM acts as hydrogen carrier.

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