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CAS

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844873-54-7

4-(tert-butoxycarbonylamino)-3-(3-cyclopentyloxy-4-methoxyphenyl)butyric acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 844873-54-7 Structure

  • Basic information

    1. Product Name: 4-(tert-butoxycarbonylamino)-3-(3-cyclopentyloxy-4-methoxyphenyl)butyric acid
    2. Synonyms: 4-(tert-butoxycarbonylamino)-3-(3-cyclopentyloxy-4-methoxyphenyl)butyric acid
    3. CAS NO:844873-54-7
    4. Molecular Formula:
    5. Molecular Weight: 393.48
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 844873-54-7.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: 4-(tert-butoxycarbonylamino)-3-(3-cyclopentyloxy-4-methoxyphenyl)butyric acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(tert-butoxycarbonylamino)-3-(3-cyclopentyloxy-4-methoxyphenyl)butyric acid(844873-54-7)
    11. EPA Substance Registry System: 4-(tert-butoxycarbonylamino)-3-(3-cyclopentyloxy-4-methoxyphenyl)butyric acid(844873-54-7)

  • 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: 844873-54-7(Hazardous Substances Data)

844873-54-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 844873-54-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,4,8,7 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 844873-54:
(8*8)+(7*4)+(6*4)+(5*8)+(4*7)+(3*3)+(2*5)+(1*4)=207
207 % 10 = 7
So 844873-54-7 is a valid CAS Registry Number.

844873-54-7Downstream Products

844873-54-7Relevant articles and documents

Synthesis of 4-aryl-2-pyrrolidones and β-aryl-γ-amino-butyric acid (GABA) analogues by Heck arylation of 3-pyrrolines with arenediazonium tetrafluoroborates. Synthesis of (±)-rolipram on a multigram scale and chromatographic resolution by semipreparative chiral simulated moving bed chromatography

Garcia, Ariel L. L.,Carpes, Marcos J. S.,De Oca, Antonio C. B. M.,Dos Santos, Marco A. G.,Santana, Cesar C.,Correia, Carlos Roque D.

, p. 1050 - 1053 (2005)

(Chemical Equation Presented) We report herein a new, practical, and economic synthesis of the phosphodiesterase inhibitor Rolipram on a multigram scale as well as the synthesis of new 4-aryl pyrrolidones and β-aryl-γ-amino butyric acids (GABA derivatives) employing an efficient Heck-Matsuda arylation of 3-pyrroline with aryldiazonium tetrafluoroborates. Racemic Rolipram was resolved into its enantiomers using chiral simulated moving bed chromatography having the low-cost microcrystalline cellulose triacetate as a chiral stationary phase.

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