Cas no 1807195-93-2 (4-Bromo-3-methyl-2-nitrobenzyl alcohol)
4-Bromo-3-methyl-2-nitrobenzyl alcohol is a brominated and nitrated benzyl alcohol derivative with a methyl substituent, offering versatile reactivity for synthetic applications. Its structure features functional groups (bromo, nitro, and hydroxyl) that enable selective transformations, making it valuable in pharmaceutical and agrochemical intermediates. The bromo and nitro groups facilitate electrophilic substitution and reduction reactions, while the benzyl alcohol moiety allows for further derivatization, such as esterification or oxidation. This compound’s well-defined reactivity profile supports its use in constructing complex aromatic frameworks. High purity grades ensure consistency in research and industrial processes, particularly in fine chemical synthesis.
1807195-93-2 structure
Product Name:4-Bromo-3-methyl-2-nitrobenzyl alcohol
CAS No:1807195-93-2
MF:C8H8BrNO3
MW:246.05802154541
CID:5001332
Update Time:2025-10-21
4-Bromo-3-methyl-2-nitrobenzyl alcohol Chemical and Physical Properties
Names and Identifiers
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- 4-Bromo-3-methyl-2-nitrobenzyl alcohol
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- Inchi: 1S/C8H8BrNO3/c1-5-7(9)3-2-6(4-11)8(5)10(12)13/h2-3,11H,4H2,1H3
- InChI Key: KVUBIACFWOQVDQ-UHFFFAOYSA-N
- SMILES: BrC1C=CC(CO)=C(C=1C)[N+](=O)[O-]
Computed Properties
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 13
- Rotatable Bond Count: 1
- Complexity: 194
- XLogP3: 1.9
- Topological Polar Surface Area: 66
4-Bromo-3-methyl-2-nitrobenzyl alcohol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A010014663-1g |
4-Bromo-3-methyl-2-nitrobenzyl alcohol |
1807195-93-2 | 97% | 1g |
1,579.40 USD | 2021-07-05 |
4-Bromo-3-methyl-2-nitrobenzyl alcohol Related Literature
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Byungho Lim,Jaewon Jin,Jin Yoo,Seung Yong Han,Kyeongyeol Kim,Sungah Kang,Nojin Park,Sang Moon Lee,Hae Jin Kim,Seung Uk Son Chem. Commun., 2014,50, 7723-7726
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Gang Pan,Yi-jie Bao,Jie Xu,Tao Liu,Cheng Liu,Yan-yan Qiu,Xiao-jing Shi,Hui Yu,Ting-ting Jia,Xia Yuan,Ze-ting Yuan,Yi-jun Cao RSC Adv., 2016,6, 42109-42119
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Norihito Fukui,Keisuke Fujimoto,Hideki Yorimitsu,Atsuhiro Osuka Dalton Trans., 2017,46, 13322-13341
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Aloke Das,K. K. Mahato,Chayan K. Nandi,Tapas Chakraborty,Shridhar R. Gadre,Nikhil A. Gokhale Phys. Chem. Chem. Phys., 2002,4, 2162-2168
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Saeideh Mirfakhraei,Malak Hekmati,Fereshteh Hosseini Eshbala,Hojat Veisi New J. Chem., 2018,42, 1757-1761
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