Welcome to LookChem.com Sign In|Join Free

CAS

  • or

29417-82-1

2-methyl-3-(3-nitrophenyl)-propionic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29417-82-1 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 29417-82-1 Structure

  • Basic information

    1. Product Name: 2-methyl-3-(3-nitrophenyl)-propionic acid methyl ester
    2. Synonyms: 2-methyl-3-(3-nitrophenyl)-propionic acid methyl ester
    3. CAS NO:29417-82-1
    4. Molecular Formula:
    5. Molecular Weight: 223.229
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 29417-82-1.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-methyl-3-(3-nitrophenyl)-propionic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-methyl-3-(3-nitrophenyl)-propionic acid methyl ester(29417-82-1)
    11. EPA Substance Registry System: 2-methyl-3-(3-nitrophenyl)-propionic acid methyl ester(29417-82-1)

  • 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: 29417-82-1(Hazardous Substances Data)

29417-82-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29417-82-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,4,1 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 29417-82:
(7*2)+(6*9)+(5*4)+(4*1)+(3*7)+(2*8)+(1*2)=131
131 % 10 = 1
So 29417-82-1 is a valid CAS Registry Number.

29417-82-1Relevant articles and documents

NaBH4-mediated facile reduction of esters of Baylis-Hillman adducts: An efficient approach to substituted propane-1,3-diols

Patra, Arundhati,Batra, Sanjay,Bhaduri, Amiya P.

, p. 1611 - 1614 (2003)

Reduction of the ester group in the Baylis-Hillman adducts by NaBH 4 reduction is facilitated by the secondary hydroxyl group present at their β-position. This method is efficient for the preparation of substituted propane-1,3-diols.

CHEMOENZYMATIC SYNTHESIS OF THE ENANTIOMERS OF IOPANOIC ACID

Colombo, M.,Amici, M. De,Micheli, C. De,Pitre, D.,Carrea, G.,Riva, S.

, p. 1021 - 1030 (2007/10/02)

The two enantiomers of Iopanoic acid 1 were prepared in enantiomeric excess higher than 90percent by enzyme-catalyzed hydrolysis of precursors (+/-)-2a and (+/-)-3a, followed by standard chemical transformations.Among the tested enzymes, chymotrypsin and Lipase PS proved to be the most selective catalysts.The stereochemical outcome of the lipase-catalyzed hydrolyses of esters (+/-)-2a-d is strictly dependent upon both the size of the alkyl group attached to the chiral center and the substituent in the aromatic ring.The enantioselectivity of the reactions was evaluated by chiral HPLC and the configurations of the new products were assigned by chemical correlations.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 29417-82-1