Skip to the beginning of the images gallery

4-Bromo-3-methylphenol - >98.0%(GC), high purity , CAS No.14472-14-1

COA

Grade & Purity:

≥98%(GC)

Cas Number: 14472-14-1
Molecular Weight: 187.03
Beilstein Registry Number: 1859122
EC Number: 238-464-3
MDL number: MFCD00079723
PubChem CID: 72857
PubChem SID: 488184720

In stock

Item Number

B124282

Grouped product items
SKU	Size	Availability	Price
B124282-1g	1g	5	$9.90
B124282-5g	5g	2	$35.90
B124282-10g	10g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$63.90
B124282-25g	25g	10	$111.90
B124282-100g	100g	6	$400.90
B124282-250g	250g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$900.90
B124282-500g	500g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$1,620.90

View related series

Oxygenated compounds (806) phenol (506)

Basic Description

Synonyms	4-bromo-5-methyl-phenol \| 4-bromo-3-methyl phenol \| 9KTP3W6RV2 \| AS-17315 \| SB33667 \| SCHEMBL49999 \| Z401597308 \| EINECS 238-464-3 \| EN300-111587 \| InChI=1/C7H7BrO/c1-5-4-6(9)2-3-7(5)8/h2-4,9H,1H \| AC-6544 \| BP-12644 \| Phenol, 4-bromo-3-methyl- \| 4-Bromo-
Specifications & Purity	≥98%(GC)
Shipped In	Normal
Product Description	description： 4-Bromo-3-methylphenol is a brominated phenol. It participates in the total synthesis of 3-methylcalix[4]arene. application： 4-Bromo-3-methylphenol may be used in the synthesis of bromo[2-methyl-4-[2-(t-butyldimethylsilyloxy)ethyloxy]phenyl]bis(triphenylphopshine)nickel(II) (protected alcohol-functionalized initiator) and bromo-[2-methyl-4-[6-(t-butyldimethylsilyloxy)hexyloxy]phenyl] bis(triphenylphosphine) nickel.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Phenols
    - Subclass Cresols

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Phenols
Subclass	Cresols
Intermediate Tree Nodes	Not available
Direct Parent	Meta cresols
Alternative Parents	P-bromophenols Toluenes Bromobenzenes 1-hydroxy-2-unsubstituted benzenoids Aryl bromides Organooxygen compounds Organobromides Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	4-halophenol - M-cresol - 4-bromophenol - Bromobenzene - Halobenzene - 1-hydroxy-2-unsubstituted benzenoid - Toluene - Aryl halide - Aryl bromide - Monocyclic benzene moiety - Organohalogen compound - Organic oxygen compound - Organobromide - Organooxygen compound - Hydrocarbon derivative - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as meta cresols. These are aromatic compounds containing a meta-cresol moiety, which consists of a benzene ring bearing a methyl group and a hydroxyl group at ring positions 1 and 3, respectively.
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	488184720
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488184720
IUPAC Name	4-bromo-3-methylphenol
INCHI	InChI=1S/C7H7BrO/c1-5-4-6(9)2-3-7(5)8/h2-4,9H,1H3
InChIKey	GPOQODYGMUTOQL-UHFFFAOYSA-N
Smiles	CC1=C(C=CC(=C1)O)Br
Isomeric SMILES	CC1=C(C=CC(=C1)O)Br
WGK Germany	3
Molecular Weight	187.03
Beilstein	1859122
Reaxy-Rn	1859122
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1859122&ln=

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

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

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

7 results found

Lot Number	Certificate Type	Date	Item
H2408173	Certificate of Analysis	Jun 14, 2024	B124282
K1427012	Certificate of Analysis	Aug 11, 2022	B124282
C2314046	Certificate of Analysis	Jun 02, 2022	B124282
G2219155	Certificate of Analysis	Jun 02, 2022	B124282
G2219169	Certificate of Analysis	Jun 02, 2022	B124282
G2219137	Certificate of Analysis	Jun 02, 2022	B124282
G2219156	Certificate of Analysis	Jun 02, 2022	B124282

Chemical and Physical Properties

Solubility	Soluble in Methanol
Boil Point(°C)	145°C/23mmHg
Melt Point(°C)	66.0-70.0°C
Molecular Weight	187.030 g/mol
XLogP3	2.000
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	0
Exact Mass	185.968 Da
Monoisotopic Mass	185.968 Da
Topological Polar Surface Area	20.200 Å²
Heavy Atom Count	9
Formal Charge	0
Complexity	94.900
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

Solution Calculators

Molarity Calculator

Determine the necessary mass, volume, or concentration for preparing a solution.

Mass

Concentration

Volume

M. Wt*

g/mol

*When preparing stock solutions, always use the batch-specific molecular weight of the product found on the vial label and the Certificate of Analysis (available online).

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Concentration 1 (C1)

Volume 1 (V1)

Concentration 2 (C2)

Volume 2 (V2)

Reconstitution Calculator

The reconstitution calculator enables you to quickly determine the volume of a reagent needed to reconstitute your vial. Just enter the mass of the reagent and the target concentration, and the calculator will do the rest.

Volume (to add to vial)

Mass (in vial)

Desired Reconstitution Concentration