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线性分子式:
NCC6H4OH
化学文摘社编号:
分子量:
119.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-259-3
Beilstein/REAXYS Number:
1210029
MDL number:
Assay:
99%
Form:
powder
产品名称
邻羟基苯甲腈, 99%
InChI key
CHZCERSEMVWNHL-UHFFFAOYSA-N
InChI
1S/C7H5NO/c8-5-6-3-1-2-4-7(6)9/h1-4,9H
SMILES string
Oc1ccccc1C#N
assay
99%
form
powder
bp
149 °C/14 mmHg (lit.)
mp
92-95 °C (lit.)
functional group
nitrile
Quality Level
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Application
2-羟基苯甲腈可用于制备:
- 甲基-(2-氰苯氧基)乙酸盐
- 3-氨基- N -苯基苯并呋喃-2-甲酰胺
- 2-(2-氧代-2-苯乙氧基)苯甲腈
- 3-氨基-2-氰基苯[ b ] 呋喃
在以下合成过程中,使用 2-羟基苯甲腈作为起始试剂:
- 单烷氧基苯基恶唑啉
- 呋喃糖苷
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Sens. 1B
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Takemoto Y, et al.
Tetrahedron, 52(45), 14177-14188 (1996)
Reactivity of 1, 2-cyclic sulfite xylosides towards nucleophiles.
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Tetrahedron, 65(43), 8858-8862 (2009)
Efficient New Synthesis of N-Arylbenzo [b] furo [3, 2-d] pyrimidin-4-amines and Their Benzo [b] thieno [3, 2-d] pyrimidin-4-amine Analogues via a Microwave-Assisted Dimroth Rearrangement.
Loidreau Y, et al.
Journal of Heterocyclic Chemistry, 50(5), 1187-1197 (2013)
meta-Selective arene C-H bond olefination of arylacetic acid using a nitrile-based directing group.
Bera M, et al.
Organic Letters, 16(21), 5760-5763 (2014)
A microwave-assisted multicomponent protocol for the synthesis of benzofuran-2-carboxamides.
Vincetti P, et al.
Tetrahedron Letters, 57(13), 1464-1467 (2016)
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