1125-31-1 | 3-Methyl-1h-indol-4-ol

Packsize	Purity	Availability	Price	Discounted Price
1mg		2 weeks	$105.00	$73.00
2mg		2 weeks	$123.00	$86.00
3mg		2 weeks	$149.00	$105.00
5mg		2 weeks	$168.00	$118.00
10mg		2 weeks	$193.00	$135.00

Description

• Catalog Number: AE54685
• Chemical Name: 3-Methyl-1h-indol-4-ol
• CAS Number: 1125-31-1
• Molecular Formula: C9H9NO
• Molecular Weight: 147.1739
• MDL Number: MFCD05668010
• SMILES: Cc1c[nH]c2c1c(O)ccc2

Computed Properties

• Complexity: 149
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 2
• XLogP3: 2.1

Upstream Synthesis Route

3-Methyl-1H-indol-4-ol, also known as $name$, is a versatile compound widely used in chemical synthesis. In organic chemistry, this compound serves as a key building block for the synthesis of various pharmaceuticals, agrochemicals, and functional materials. One of the primary applications of 3-Methyl-1H-indol-4-ol is in the preparation of indole derivatives, which are important structural motifs found in numerous bioactive compounds. By functionalizing the indole ring of this compound through various chemical reactions, chemists can access a diverse array of molecules with potential therapeutic properties.Furthermore, 3-Methyl-1H-indol-4-ol can be utilized in the synthesis of natural products and complex molecules with biological activity. Its unique structural features allow for selective modifications that enable the creation of novel compounds for drug discovery and development.Overall, the versatility of 3-Methyl-1H-indol-4-ol in chemical synthesis makes it a valuable tool for organic chemists seeking to access a wide range of structurally diverse compounds with potential applications in pharmaceuticals, agriculture, and materials science.

Literature

• Resynthesized lines and cultivars of Brassica napus L. provide sources of resistance to the cabbage stem weevil ( Ceutorhynchus pallidactylus (Mrsh.)).

  Bulletin of entomological research 20110601

• Metabolic engineering in Nicotiana benthamiana reveals key enzyme functions in Arabidopsis indole glucosinolate modification.

  The Plant cell 20110201

• Whole genome co-expression analysis of soybean cytochrome P450 genes identifies nodulation-specific P450 monooxygenases.

  BMC plant biology 20100101

• Mapping of QTL for resistance against the crucifer specialist herbivore Pieris brassicae in a new Arabidopsis inbred line population, Da(1)-12 x Ei-2.

  PloS one 20070101