145747-16-6

• 

• Basic information

  1. Product Name: methoxyacetic acid, hexyl ester
  2. Synonyms:
  3. CAS NO:145747-16-6
  4. Molecular Formula:
  5. Molecular Weight: 174.24
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 145747-16-6.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: methoxyacetic acid, hexyl ester(CAS DataBase Reference)
  10. NIST Chemistry Reference: methoxyacetic acid, hexyl ester(145747-16-6)
  11. EPA Substance Registry System: methoxyacetic acid, hexyl ester(145747-16-6)

• 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: 145747-16-6(Hazardous Substances Data)

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• Hexyl2-methoxyacetate

  Cas No: 145747-16-6

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• methoxyacetic acid, hexyl ester

  Cas No: 145747-16-6

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145747-16-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145747-16-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,7,4 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 145747-16:
(8*1)+(7*4)+(6*5)+(5*7)+(4*4)+(3*7)+(2*1)+(1*6)=146
146 % 10 = 6
So 145747-16-6 is a valid CAS Registry Number.

145747-16-6Upstream product

• 111-27-3 hexan-1-ol 

145747-16-6Downstream Products

145747-16-6Relevant articles and documents

Rate enhancement of the Candida cylindracea lipase catalysed transesterification in organic solvents: Enzymatic reactions below zero

Hogan, V F,O'Hagan, D,Sanvoisin, J

, p. 883 - 885 (2007/10/02)

The rate of transesterification reactions of primary and secondary alcohols, catalysed by the lipase from Candida cylindracea in organic solvents, can be accelerated when methoxyacyl is the transacylating group in the transacylating agent.This phenomenon allows efficient transesterifications to be catalysed at temperatures below zero degree.

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