147330-13-0

• 

• Basic information

  1. Product Name: Carbamic acid, 4-cycloocten-1-yl-, methyl ester (9CI)
  2. Synonyms: Carbamic acid, 4-cycloocten-1-yl-, methyl ester (9CI)
  3. CAS NO:147330-13-0
  4. Molecular Formula: C10H17NO2
  5. Molecular Weight: 183.25
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 147330-13-0.mol
  9. Article Data: 2

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: Carbamic acid, 4-cycloocten-1-yl-, methyl ester (9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: Carbamic acid, 4-cycloocten-1-yl-, methyl ester (9CI)(147330-13-0)
  11. EPA Substance Registry System: Carbamic acid, 4-cycloocten-1-yl-, methyl ester (9CI)(147330-13-0)

• 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: 147330-13-0(Hazardous Substances Data)

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147330-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147330-13-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,3,3 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 147330-13:
(8*1)+(7*4)+(6*7)+(5*3)+(4*3)+(3*0)+(2*1)+(1*3)=110
110 % 10 = 0
So 147330-13-0 is a valid CAS Registry Number.

147330-13-0Upstream product

• 67-56-1 methanol 
• 4103-13-3 4-cyclooctene-1-carboxamide 
• 70423-71-1 (Z)-cyclooct-4-en-1-amine 
• 79-22-1 methyl chloroformate 
• 31598-70-6 cis-cyclooct-4-enone 
• 68344-35-4 cyclooct-4-enone oxime 

147330-13-0Downstream Products

147330-13-0Relevant articles and documents

A formal total synthesis of (±)-anatoxin-a by an intramolecular Pd- catalyzed aminocarbonylation reaction

Oh, Chang-Young,Kim, Kee-Soo,Ham, Won-Hun

, p. 2133 - 2136 (2007/10/03)

9-Azabicyclo[4.2.1]nonane skeleton 3a was prepared by intramolecular aminocarbonylation of 2a catalyzed by palladium. In three steps 3a was transformed into 8 which had previously been transformed into anatoxin-a, thus completing the formal total synthesis.

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