Welcome to LookChem.com Sign In|Join Free
  • or
(2R,3R)-2-Phenyl-2,3-dihydro-1H-pyrrole-3,4-dicarboxylic acid dimethyl ester is a complex organic compound with the molecular formula C14H15NO4. It is a chiral molecule, meaning it has a non-superimposable mirror image, and the specific configuration is indicated by the (2R,3R) notation. (2R,3R)-2-Phenyl-2,3-dihydro-1H-pyrrole-3,4-dicarboxylic acid dimethyl ester features a pyrrole ring, which is a five-membered aromatic ring containing one nitrogen atom, and is fused to a dihydro structure. The molecule also contains two carboxylic acid groups at the 3 and 4 positions, which are esterified with methanol, resulting in dimethyl ester groups. This chemical structure endows the compound with specific properties and potential applications in various fields, such as pharmaceuticals or materials science, where its unique stereochemistry and functional groups can be exploited.

69994-52-1

Post Buying Request

69994-52-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

69994-52-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69994-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,9,9 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69994-52:
(7*6)+(6*9)+(5*9)+(4*9)+(3*4)+(2*5)+(1*2)=201
201 % 10 = 1
So 69994-52-1 is a valid CAS Registry Number.

69994-52-1Downstream Products

69994-52-1Relevant academic research and scientific papers

Metallic Base-Induced Cycloadditions of N-(1-Cyanoalkyl)imines via N-Metalated Azomethine Ylides: Enhanced Reactivity and High Regio- and Stereoselectivity

Tsuge, Otohiko,Kanemasa, Shuji,Yorozu, Kiyotaka,Ueno, Kazunori

, p. 3359 - 3366 (2007/10/02)

Lithiation of N-(1-cyanoalkyl)imines with LDA generates new N-lithiated azomethine ylide 1,3-dipoles which show enhanced reactivity toward dipolarophiles.They undergo exclusively regio- and stereoselective 3+2 cycloaddition reaction with α,β-unsaturated e

Stereoselectivity of Cycloaddition of N-(Cyanomethyl)- and N-(α-Cyanobenzyl)imines with Olefinic Dipolarophiles. Synthetic Equivalents of Nitrile Ylide 1,3-Dipoles

Tsuge, Otohiko,Ueno, Kazunori,Kanemasa, Shuji,Yorozu, Kiyotaka

, p. 1809 - 1824 (2007/10/02)

N-(Cyanomethyl)- and N-(α-cyanobenzyl)imines derived from a variety of aldehydes and ketones can tautomerize into N-protonated azomethine ylides which undergo cycloadditions with olefinic dipolarophiles.These cycloadditions are often accompanied by the el

CYCLOADDITIONS OF N-BENZYLIDENEAMINOACETONITRILE AS A SYNTHETIC EQUIVALENT OF METHANENITRILE BENZZLIDE

Tsuge, Otohiko,Kanemasa, Shuji,Yorozu, Kiyotaka,,Ueno, Kazunori

, p. 1601 - 1604 (2007/10/02)

N-Benzylideneaminoacetonitrile is a synthetic equivalent of methanenitrile benzylide via a cycloaddition and elimination sequence.Its reactions with olefinic dipolarophiles provide stereochemically defined 1- or 2-pyrrolines.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 69994-52-1