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CAS

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1352831-33-4

(S)-2-methoxy-3-(4-methoxyphenyl)propanal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1352831-33-4 Structure

  • Basic information

    1. Product Name: (S)-2-methoxy-3-(4-methoxyphenyl)propanal
    2. Synonyms:
    3. CAS NO:1352831-33-4
    4. Molecular Formula:
    5. Molecular Weight: 194.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1352831-33-4.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: (S)-2-methoxy-3-(4-methoxyphenyl)propanal(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-2-methoxy-3-(4-methoxyphenyl)propanal(1352831-33-4)
    11. EPA Substance Registry System: (S)-2-methoxy-3-(4-methoxyphenyl)propanal(1352831-33-4)

  • 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: 1352831-33-4(Hazardous Substances Data)

1352831-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1352831-33-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,2,8,3 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1352831-33:
(9*1)+(8*3)+(7*5)+(6*2)+(5*8)+(4*3)+(3*1)+(2*3)+(1*3)=144
144 % 10 = 4
So 1352831-33-4 is a valid CAS Registry Number.

1352831-33-4Downstream Products

1352831-33-4Relevant articles and documents

Productivity enhancement of CC bioreductions by coupling the in situ substrate feeding product removal technology with isolated enzymes

Brenna, Elisabetta,Gatti, Francesco G.,Monti, Daniela,Parmeggiani, Fabio,Sacchetti, Alessandro

supporting information; experimental part, p. 79 - 81 (2012/01/12)

To overcome the usually low productivities of the CC bond bioreduction of α,β-unsaturated aldehydes we combined the in situ substrate feeding product removal (SFPR) technology with a cascade system comprising an isolated ene-reductase and a chemoselective alcohol dehydrogenase.

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