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1429373-35-2

2-ethoxycarbonyloxy-(R)-2-(4-tert-butylphenyl)-acetonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1429373-35-2 Structure

  • Basic information

    1. Product Name: 2-ethoxycarbonyloxy-(R)-2-(4-tert-butylphenyl)-acetonitrile
    2. Synonyms:
    3. CAS NO:1429373-35-2
    4. Molecular Formula:
    5. Molecular Weight: 261.321
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1429373-35-2.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-ethoxycarbonyloxy-(R)-2-(4-tert-butylphenyl)-acetonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-ethoxycarbonyloxy-(R)-2-(4-tert-butylphenyl)-acetonitrile(1429373-35-2)
    11. EPA Substance Registry System: 2-ethoxycarbonyloxy-(R)-2-(4-tert-butylphenyl)-acetonitrile(1429373-35-2)

  • 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: 1429373-35-2(Hazardous Substances Data)

1429373-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1429373-35-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,9,3,7 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1429373-35:
(9*1)+(8*4)+(7*2)+(6*9)+(5*3)+(4*7)+(3*3)+(2*3)+(1*5)=172
172 % 10 = 2
So 1429373-35-2 is a valid CAS Registry Number.

1429373-35-2Downstream Products

1429373-35-2Relevant articles and documents

Asymmetric Carboxycyanation of Aldehydes by Cooperative AlF/Onium Salt Catalysts: from Cyanoformate to KCN as Cyanide Source

Brodbeck, Daniel,álvarez-Barcia, Sonia,Meisner, Jan,Broghammer, Florian,Klepp, Julian,Garnier, Delphine,Frey, Wolfgang,K?stner, Johannes,Peters, René

, p. 1515 - 1524 (2019)

Asymmetric 1,2-additions of cyanide yield enantioenriched cyanohydrins as versatile chiral building blocks. Next to HCN, volatile organic cyanide sources are usually used. Among them, cyanoformates are more attractive on technical scale than TMSCN for cos

Bifunctional Schiff base/Ti(IV) catalysts for enantioselective cyanoformylation of aldehydes with ethyl cyanoformate

Ji, Nan,Yao, Lin,He, Wei,Li, Yurong

, p. 209 - 213 (2013/05/08)

A new bifunctional titanium/Schiff base catalyst was developed for the enantioselective cyanoformylation of aldehydes with ethyl cyanoformate. The reaction proceeded smoothly with a mild reaction condition to afford the cyanohydrin ethyl carbonates in hig

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