Date published: 2026-5-9

1-800-457-3801

SCBT Portrait Logo
Seach Input

m-Tolunitrile (CAS 620-22-4)

0.0(0)
Write a reviewAsk a question

Alternate Names:
3-Methylbenzonitrile
CAS Number:
620-22-4
Molecular Weight:
117.15
Molecular Formula:
C8H7N
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

m-Tolunitrile is a versatile organic compound with the molecular formula C8H7N. It appears as a colorless, aromatic oily liquid, boasting a distinctive scent. This compound serves as a valuable starting material for a wide array of organic compounds, making it highly sought-after in scientific research. Scientists harness the capabilities of m-Tolunitrile across diverse research applications. Its significance extends to organic synthesis, where it acts as a foundational component in generating fragrances and dyes. Additionally, m-Tolunitrile finds application in photochemistry, serving as a photosensitizer in photochemical reactions. Being an aromatic compound, m-Tolunitrile partakes in several intriguing reactions, encompassing nucleophilic substitution, electrophilic substitution, and radical substitution. In nucleophilic substitution, the compound reacts with nucleophiles like bases or acids, culminating in the formation of novel products. On the other hand, electrophilic substitution involves its interaction with electron-deficient species, leading to the creation of fresh products. Lastly, radical substitution reactions involve 3-Methylbenzonitrile′s response to radicals, including free radicals, resulting in the synthesis of new products.


m-Tolunitrile (CAS 620-22-4) References

  1. The Microwave Spectrum of m-Tolunitrile: Methyl Internal Rotation and (14)N Nuclear Quadrupole Coupling.  |  Bruhn, T. and Mäder, H. 2000. J Mol Spectrosc. 200: 151-161. PMID: 10708528
  2. Absolute orientation of molecules at interfaces.  |  Rao, Y., et al. 2006. J Phys Chem B. 110: 1727-32. PMID: 16471739
  3. An amino acid at position 142 in nitrilase from Rhodococcus rhodochrous ATCC 33278 determines the substrate specificity for aliphatic and aromatic nitriles.  |  Yeom, SJ., et al. 2008. Biochem J. 415: 401-7. PMID: 18412544
  4. Formation of fullerooxazoles from C61HPh(3-): the regioselectivity of heteroatom additions.  |  Li, FF., et al. 2009. J Org Chem. 74: 8071-7. PMID: 19791758
  5. Isolation and Characterization of a Nitrile-Hydrolysing Bacterium Isoptericola variabilis RGT01.  |  Kaur, G., et al. 2014. Indian J Microbiol. 54: 232-8. PMID: 25320428

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

m-Tolunitrile, 100 g

sc-235539
100 g
$43.00