4-Isopropylphenylboronic Acid
Product Information
Molecular Formula
C9H13O2B
Molecular Weight
164.01
Description
4-Isopropylphenylboronic Acid (CAS# 16152-51-5) is used as a reactant for the preparation of furan-2-carbohydrazides as orally active glucagon receptor antagonists.
Synonyms
(4-propan-2-ylphenyl)boronic acid; (4-propan-2-ylphenyl)boronic acid
IUPAC Name
(4-propan-2-ylphenyl)boronic acid
SMILES
B(C1=CC=C(C=C1)C(C)C)(O)O
InChI
InChI=1S/C9H13BO2/c1-7(2)8-3-5-9(6-4-8)10(11)12/h3-7,11-12H,1-2H3
InChI Key
IAEUFBDMVKQCLU-UHFFFAOYSA-N
Boiling Point
285.9 °C at 760 mmHg
Flash Point
Not applicable
Density
1.04 g/cm3
LogP
0.48980
Safety Information
Hazards
H302 - H317
Precautionary Statement
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501
Signal Word
Warning
Computed Properties
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
2
Exact Mass
164.1008598 g/mol
Monoisotopic Mass
164.1008598 g/mol
Topological Polar Surface Area
40.5Ų
Heavy Atom Count
12
Formal Charge
0
Complexity
129
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| CN-113930790-A | Synthetic method of aryl selenide compound | 2021-09-07 |
| CN-113549081-A | Organic compound and organic electroluminescent device using same | 2021-07-26 |
| CN-113402412-A | (E) Method for synthesizing (beta) -fluoroacrylamide derivative | 2021-06-10 |
| CN-112961140-A | Naphthoquinone heterocyclic compound and application thereof | 2021-02-08 |
| CN-112625042-A | Organic electroluminescent material and application thereof | 2020-12-28 |
| CN-112409241-A | Organic compound, application thereof and organic electroluminescent device adopting organic compound | 2020-11-27 |
| CN-112480160-A | Second-order silane derivative, chiral third-order silane derivative, preparation method of chiral fourth-order silane derivative and chiral product of chiral fourth-order silane derivative | 2020-10-20 |
| CN-112480160-B | Second-order silane derivative, chiral third-order silane derivative, preparation method of chiral fourth-order silane derivative and chiral product of chiral fourth-order silane derivative | 2020-10-20 |
| WO-2022038116-A1 | N-hydroxycarboxamide derivatives useful as inhibitors of mammalian histone deacetylase activity | 2020-08-19 |
| CN-111875618-A | Compound with multi-heterocyclic structure and application thereof | 2020-07-31 |
