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Cyclopropylboronic acid（contains varying amounts of Anhydride） - 90%, high purity , CAS No.411235-57-9

COA

Grade & Purity:

≥90%

Cas Number: 411235-57-9
Molecular Weight: 85.9
MDL number: MFCD04038750
PubChem CID: 2760897
PubChem SID: 504761589

In stock

Item Number

C120273

Grouped product items
SKU	Size	Availability	Price
C120273-1g	1g	1	$86.90
C120273-5g	5g	3	$242.90
C120273-10g	10g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$436.90
C120273-25g	25g	3	$981.90
C120273-100g	100g	2	$3,532.90
C120273-500g	500g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$15,894.90

Basic Description

Synonyms	CYCLOPROPANEBORONIC ACID \| cyclopropanylboronic acid \| cyclopropyboronic acid \| AM20100093 \| A6833 \| BP-10013 \| cylcopropylboronic acid \| DTXSID00375402 \| AC-6414 \| cycloproyl boronic acid \| HY-59219 \| STL558619 \| cyclopropylboranediol \| Cyclopropylboroni
Specifications & Purity	≥90%
Storage Temp	Store at -20°C,Argon charged
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Cyclopropylboronic acid is a useful building block in Suzuki coupling. Cyclopropylboronic acid contains varying amounts of anhydride. Reagent used for: 1.Microwave-assisted copper(II)-catalyzed N-cyclopropylation. 2.Nickel- and copper-catalyzed Suzuki-Miyaura coupling reaction of arenes. 3.Palladacycle-catalyzed Suzuki-cross coupling of aryl halides with cyclopropylboronic acid. 4.Palladium(0)-catalyzed cyclopropane C-H bond functionalization. 5.Palladium-catalyzed decarboxylative coupling. 6.Palladium-catalyzed ligand-directed oxidative functionalization of cyclopropanes. 7.Palladium-catalyzed Suzuki coupling reaction. Reagent used in Preparation of: 1.Diaryl ketones by arylation of arylboronic acids with aromatic aldehydes catalyzed by Cu(OTf)2 and Xantphos. 2.Aminothiazolylpyrrolidine-based tartrate diamides as TACE inhibitors to treat inflammatory disorders and cancer.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Class Boronic acid derivatives
    - Subclass Boronic acids

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Class	Boronic acid derivatives
Subclass	Boronic acids
Intermediate Tree Nodes	Not available
Direct Parent	Boronic acids
Alternative Parents	Organic metalloid salts Organic oxygen compounds Monoalkylboranes Hydrocarbon derivatives
Molecular Framework	Aliphatic homomonocyclic compounds
Substituents	Boronic acid - Organic metalloid salt - Organic oxygen compound - Monoalkylborane - Alkylborane - Hydrocarbon derivative - Organic salt - Organoboron compound - Aliphatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as boronic acids. These are compounds comprising the boronic acid functional group RB(O)O (R,R'=alkyl, aryl).
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

Pubchem Sid	504761589
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504761589
IUPAC Name	cyclopropylboronic acid
INCHI	InChI=1S/C3H7BO2/c5-4(6)3-1-2-3/h3,5-6H,1-2H2
InChIKey	WLVKDFJTYKELLQ-UHFFFAOYSA-N
Smiles	B(C1CC1)(O)O
Isomeric SMILES	B(C1CC1)(O)O
WGK Germany	3
Molecular Weight	85.9
Reaxy-Rn	9385789
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=9385789&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

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6 results found

Lot Number	Certificate Type	Date	Item
L2425459	Certificate of Analysis	Jul 12, 2024	C120273
F1523102	Certificate of Analysis	Aug 04, 2023	C120273
J1910122	Certificate of Analysis	Jul 06, 2023	C120273
I2206437	Certificate of Analysis	Jun 30, 2022	C120273
I2206518	Certificate of Analysis	Jun 30, 2022	C120273
I2206519	Certificate of Analysis	Jun 30, 2022	C120273

Chemical and Physical Properties

Sensitivity	Hygroscopic
Melt Point(°C)	90-95°C
Molecular Weight	85.900 g/mol
XLogP3
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	1
Exact Mass	86.0539 Da
Monoisotopic Mass	86.0539 Da
Topological Polar Surface Area	40.500 Å²
Heavy Atom Count	6
Formal Charge	0
Complexity	50.800
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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