160030-82-0

• 

• Basic information

  1. Product Name: Acetic acid, [(diphenylmethyl)oxidoimino]-, methyl ester
  2. Synonyms:
  3. CAS NO:160030-82-0
  4. Molecular Formula: C16H15NO3
  5. Molecular Weight: 269.3
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 160030-82-0.mol
  9. Article Data: 1

• 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: Acetic acid, [(diphenylmethyl)oxidoimino]-, methyl ester(CAS DataBase Reference)
  10. NIST Chemistry Reference: Acetic acid, [(diphenylmethyl)oxidoimino]-, methyl ester(160030-82-0)
  11. EPA Substance Registry System: Acetic acid, [(diphenylmethyl)oxidoimino]-, methyl ester(160030-82-0)

• 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: 160030-82-0(Hazardous Substances Data)

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160030-82-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 160030-82-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,0,3 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 160030-82:
(8*1)+(7*6)+(6*0)+(5*0)+(4*3)+(3*0)+(2*8)+(1*2)=80
80 % 10 = 0
So 160030-82-0 is a valid CAS Registry Number.

160030-82-0Upstream product

• 922-68-9 Methyl glyoxylate 
• 1485-71-8 benzophenone oxime 

160030-82-0Downstream Products

• 81102-35-4 2-Benzhydryl-5-formyl-isoxazolidine-3-carboxylic acid methyl ester 

160030-82-0Relevant articles and documents

Studies on tandem transesterification and intramolecular cycloaddition of nitrones. 1. Sequential bicyclization of α-methoxycarbonylnitrones with allyl alcohols

Tamura, Osamu,Okabe, Toshiyuki,Yamaguchi, Tatsuya,Gotanda, Kentoku,Noe, Katsuhide,Sakamoto, Masanori

, p. 107 - 118 (2007/10/02)

Treatment of α-methoxycarbonylnitrones with 5 equiv. of allyl alcohols in the presence of 1 equiv. of titanium tetraisopropoxide causes tandem transesterification, E,Z-isomerization of the nitrone moieties, and intramolecular cycloaddition to afford bicyclized compounds in one step. To reduce amounts of allyl alcohol, combined use of a catalytic amount of titanium tetraisopropoxide and molecular sieves 4A was found to be a more improved catalytic system. It was also found that reactions of (Z)-allyl alcohols with α-methoxycarbonylnitrone are more facile than those of (E)-allyl alcohols. This aspect was extended to geometry differentiated cycloaddition.

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