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Safety Information

385409

Sigma-Aldrich

4-Bromo-3-methylanisole

98%

Synonym(s):

2-Bromo-5-methoxytoluene

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About This Item

Linear Formula:
BrC6H3(CH3)OCH3
CAS Number:
27060-75-9
Molecular Weight:
201.06
MDL number:
MFCD00060687
UNSPSC Code:
12352100
PubChem Substance ID:
24864024
NACRES:
NA.22

Quality Level

100

Assay

98%

form

liquid

refractive index

n20/D 1.561 (lit.)

bp

111-112 °C/15 mmHg (lit.)

solubility

water: soluble (Partially miscible)(lit.)

density

1.424 g/mL at 25 °C (lit.)

functional group

bromo

SMILES string

COc1ccc(Br)c(C)c1

InChI

1S/C8H9BrO/c1-6-5-7(10-2)3-4-8(6)9/h3-5H,1-2H3

InChI key

BLZNSXFQRKVFRP-UHFFFAOYSA-N

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

385409-5ML:
385409-25ML:
385409-BULK:
385409-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
STBJ8186
STBH0996
MKBB4423
62797KJ
U15437

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The synthesis of (?)-aplysin and (?)-debromoaplysin.
<BIG>Yamada et al. </BIG>
Chemical Communications (Cambridge, England), 22, 1432-1432 (1968)
A concise synthesis of the naphthoic acid component of neocarzinostatin chromophore featuring a new photocyclization reaction.
Myers et al.
Tetrahedron Letters, 37.5, 587-590 (1996)
Discovery of orally active nonpeptide vitronectin receptor antagonists based on a 2-benzazepine Gly-Asp mimetic.
W H Miller et al.
Journal of medicinal chemistry, 43(1), 22-26 (2000-01-14)
Effect of cyclodextrins on electrophilic aromatic bromination in aqueous solution.
<BIG>Dumanski et al.</BIG>
Australian Journal of Chemistry, 56(11), 1107-1111 (2003)
Lucas R Moore et al.
Organic letters, 6(2), 225-228 (2004-01-16)
[reaction: see text] Sterically demanding, sulfonated arylphosphines TXPTS and TMAPTS have been applied to the aqueous-phase Heck and Suzuki coupling of aryl bromides. TXPTS provides good yields of Heck coupling products from aryl bromides at 80 degrees C, while both

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