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CAS

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636572-24-2

2-Propenoic acid, (2S)-2-[[4-(4-iodophenyl)butyl](phenylmethyl)amino]-3-methylbutyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 636572-24-2 Structure

  • Basic information

    1. Product Name: 2-Propenoic acid, (2S)-2-[[4-(4-iodophenyl)butyl](phenylmethyl)amino]-3-methylbutyl ester
    2. Synonyms:
    3. CAS NO:636572-24-2
    4. Molecular Formula: C25H32INO2
    5. Molecular Weight: 505.439
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 636572-24-2.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: 2-Propenoic acid, (2S)-2-[[4-(4-iodophenyl)butyl](phenylmethyl)amino]-3-methylbutyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Propenoic acid, (2S)-2-[[4-(4-iodophenyl)butyl](phenylmethyl)amino]-3-methylbutyl ester(636572-24-2)
    11. EPA Substance Registry System: 2-Propenoic acid, (2S)-2-[[4-(4-iodophenyl)butyl](phenylmethyl)amino]-3-methylbutyl ester(636572-24-2)

  • 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: 636572-24-2(Hazardous Substances Data)

636572-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 636572-24-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,6,5,7 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 636572-24:
(8*6)+(7*3)+(6*6)+(5*5)+(4*7)+(3*2)+(2*2)+(1*4)=172
172 % 10 = 2
So 636572-24-2 is a valid CAS Registry Number.

636572-24-2Relevant articles and documents

A versatile approach to chiral macrocycles

Gibson, Susan E.,Mainolfi, Nello,Kalindjian, S. Barret,Wright, Paul T.

, p. 1568 - 1569 (2003)

Head-to-tail Heck coupling of units derived from amino alcohols and iodoaryl aldehydes provides a short and versatile route to non-racemic chiral macrocycles.

A new class of non-racemic chiral macrocycles: A conformational and synthetic study

Gibson, Susan E.,Mainolfi, Nello,Kalindjian, S. Barret,Wright, Paul T.,White, Andrew J. P.

, p. 69 - 80 (2007/10/03)

Amino alcohols have been used to introduce non-racemic chirality into macrocycles using a modular approach that relies on a Heck macrocyclisation reaction. A wide variety of macrocycles have been synthesised, and their structures studied using X-ray crystallography and molecular modelling. A fragmentation reaction encountered during the use of (S)-1,1-dimethylvalinol revealed that carboxylic acids generate acylals under reaction conditions often used for Heck reactions.

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