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

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  • 1262832-35-8 Structure
  • Basic information

    1. Product Name: 3-(2-methoxyphenyl)-2,2-dimethyl-4-nitrobutanal
    2. Synonyms:
    3. CAS NO:1262832-35-8
    4. Molecular Formula:
    5. Molecular Weight: 251.282
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1262832-35-8.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: 3-(2-methoxyphenyl)-2,2-dimethyl-4-nitrobutanal(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(2-methoxyphenyl)-2,2-dimethyl-4-nitrobutanal(1262832-35-8)
    11. EPA Substance Registry System: 3-(2-methoxyphenyl)-2,2-dimethyl-4-nitrobutanal(1262832-35-8)
  • 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: 1262832-35-8(Hazardous Substances Data)

1262832-35-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1262832-35-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,8,3 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1262832-35:
(9*1)+(8*2)+(7*6)+(6*2)+(5*8)+(4*3)+(3*2)+(2*3)+(1*5)=148
148 % 10 = 8
So 1262832-35-8 is a valid CAS Registry Number.

1262832-35-8Downstream Products

1262832-35-8Relevant articles and documents

Asymmetric Michael reaction between aldehydes and nitroalkanes promoted by pyrrolidine-containing C2-symmetric organocatalysts

Bykova,Kostenko,Kucherenko,Zlotin

, p. 1402 - 1406 (2019)

Bifunctional C2-symmetric organocatalysts derived from chiral 1,2-diaminoethanes and (S)-2-aminomethylpyrrolidine were fi rst used for promoting the asymmetric Michael addition of aliphatic aldehydes to nitroalkenes. The synthesized enantioenri

Practical access to highly enantioenriched quaternary carbon Michael adducts using simple organocatalysts

Nugent, Thomas C.,Shoaib, Mohammad,Shoaib, Amna

supporting information; experimental part, p. 52 - 56 (2011/02/24)

A three component catalyst system entailing an amino acid (O tBu-l-threonine), a hydrogen bond donor (sulfamide), and an amine base (DMAP) allows α-branched aldehyde addition to nitroalkenes in good to high yield and excellent ee. Importantly,

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