CAS 2972-82-9

2-(1,3-Benzodioxol-5-ylmethylene)propanedinitrile

Description:

2-(1,3-Benzodioxol-5-ylmethylene)propanedinitrile, with the CAS number 2972-82-9, is an organic compound characterized by its unique structure that includes a benzodioxole moiety and a propanedinitrile group. This compound typically appears as a crystalline solid and is known for its potential applications in organic synthesis and as an intermediate in the production of various chemical entities. The presence of the dinitrile functional groups contributes to its reactivity, making it a useful building block in the synthesis of more complex molecules. Additionally, the benzodioxole ring system imparts certain electronic properties, which can influence the compound's behavior in chemical reactions. Its solubility can vary depending on the solvent, and it may exhibit fluorescence or other photophysical properties. Safety data should be consulted, as with any chemical, to understand its handling, storage, and potential hazards. Overall, this compound is of interest in both academic research and industrial applications due to its versatile chemical properties.

Formula: C₁₁H₆N₂O₂

InChI: InChI=1/C11H6N2O2/c12-5-9(6-13)3-8-1-2-10-11(4-8)15-7-14-10/h1-4H,7H2

InChI key: InChIKey=AWMFEYQOEQDZKO-UHFFFAOYSA-N

SMILES: C(=C(C#N)C#N)C=1C=C2C(=CC1)OCO2

Synonyms:

• (1,3-Benzodioxol-5-Ylmethylidene)Propanedinitrile
• (1,3-Benzodioxol-5-ylmethylene)malononitrile
• (1,3-Benzodioxol-5-ylmethylene)propanedinitrile
• (Benzo[3,4-d]1,3-dioxolan-5-ylmethylene)methane-1,1-dicarbonitrile
• 2-((Benzo[d][1,3]dioxol-5-yl)methylene)malononitrile
• 2-(1,3-Benzodioxol-5-ylmethylene)propanedinitrile
• 2-(1,3-Benzodioxol-5-ylmethylidene)propanedinitrile
• 2-(2H-1,3-Benzodioxol-5-ylmethylidene)propanedinitrile
• 2-[(2H-1,3-Benzodioxol-5-yl)methylidene]propanedinitrile
• 3,4-Methylenedioxyphenylmethylenemalononitrile
• 3-(1,3-Benzodioxol-5-yl)-2-cyanopropenenitrile
• Brn 0181717
• Malononitrile, (piperonylidene)-
• Nsc 1340
• Nsc 521577
• Piperonalmalononitrile
• Piperonylidenemalononitrile
• Propanedinitrile, (1,3-benzodioxol-5-ylmethylene)-
• Propanedinitrile, 2-(1,3-benzodioxol-5-ylmethylene)-
• [3,4-(Methylenedioxy)benzylidene]malononitrile
• 5-19-07-00480 (Beilstein Handbook Reference)
• AKOS BBS-00000848
• RARECHEM AL BX 0548
• 2-(Benzo[d][1,3]dioxol-5-ylmethylene)malononitrile
• 2-BENZO[1,3]DIOXOL-5-YLMETHYLENE-MALONONITRILE

PROPANEDINITRILE, 2-(1,3-BENZODIOXOL-5-YLMETHYLENE)-

CAS: 2972-82-9

Formula: C₁₁H₆N₂O₂

Purity: 95%

Molecular weight: 198.1775

Ref: IN-DA002Z8H

2-(Benzo[d][1,3]dioxol-5-ylmethylene)malononitrile

CAS: 2972-82-9

2-(Benzo[d][1,3]dioxol-5-ylmethylene)malononitrile

Purity: 97%

Molecular weight: 198.18g/mol

Ref: 54-OR1075612

(Benzo[3,4-d]1,3-dioxolan-5-ylmethylene)methane-1,1-dicarbonitrile

CAS: 2972-82-9

Purity: 95.0%

Color and Shape: Solid

Molecular weight: 198.18099975585938

Ref: 10-F068951

(benzo[3,4-d]1,3-dioxolan-5-ylmethylene)methane-1,1-dicarbonitrile

CAS: 2972-82-9

Benzo[3,4-d]1,3-dioxolan-5-ylmethylene)methane-1,1-dicarbonitrile (BD) is a synthetic antibiotic that has been found to have antimicrobial activity against gram-negative bacteria. It inhibits the growth of these bacteria by binding to DNA and inhibiting the synthesis of proteins. BD is similar in structure to chloramphenicol, which also has inhibitory effects on protein synthesis and binds to DNA. However, BD does not bind as well as chloramphenicol to the 50S ribosomal subunit, preventing it from inhibiting protein synthesis. This lack of inhibition may be due to a higher affinity for aromatic amines than chloramphenicol has.

Formula: C₁₁H₆N₂O₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 198.18 g/mol

Ref: 3D-FB169463