14257-49-9

• 

• Basic information

  1. Product Name: N-(CYCLOHEXANEMETHYL) ASPARTIC ACID
  2. Synonyms: N-(CYCLOHEXANEMETHYL) ASPARTIC ACID
  3. CAS NO:14257-49-9
  4. Molecular Formula: C₁₁H₁₉NO₄
  5. Molecular Weight: 229.27
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 14257-49-9.mol
  9. Article Data: 1

• 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: N-(CYCLOHEXANEMETHYL) ASPARTIC ACID(CAS DataBase Reference)
  10. NIST Chemistry Reference: N-(CYCLOHEXANEMETHYL) ASPARTIC ACID(14257-49-9)
  11. EPA Substance Registry System: N-(CYCLOHEXANEMETHYL) ASPARTIC ACID(14257-49-9)

• 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: 14257-49-9(Hazardous Substances Data)

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14257-49-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14257-49-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,5 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14257-49:
(7*1)+(6*4)+(5*2)+(4*5)+(3*7)+(2*4)+(1*9)=99
99 % 10 = 9
So 14257-49-9 is a valid CAS Registry Number.

14257-49-9Upstream product

• 108-31-6 maleic anhydride 
• 3218-02-8 cyclohexylmethylamine 

14257-49-9Downstream Products

14257-49-9Relevant articles and documents

Direct synthesis of N-substituted, functionalized aspartic acids using alkali maleates and amines

Piispanen, Peter S.,Pihko, Petri M.

, p. 2751 - 2755 (2007/10/03)

A practical and general one-pot synthesis of mono-N-substituted, functionalized aspartic acids has been developed. The N-substituted aspartic acids are formed directly from alkali maleates and primary amines in hot DMSO. Products from several different primary amines can be prepared chemoselectively in moderate to good yields.

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