Skip to Content
Merck
All Photos(3)

Key Documents

View All Documentation

Safety Information

180637

Sigma-Aldrich

9-Hydroxy-9-fluorenecarboxylic acid

96%

Synonym(s):

Flurenol, 9-Hydroxyfluorene-9-carboxylic acid

Sign Into View Organizational & Contract Pricing

Select a Size

5 G
¥4,120
25 G
¥15,800

¥4,120

0 left in stock
Request a Bulk Order
All Photos(3)

Select a Size

Change View
5 G
¥4,120
25 G
¥15,800

About This Item

Empirical Formula (Hill Notation):
C14H10O3
CAS Number:
467-69-6
Molecular Weight:
226.23
Beilstein:
1314711
EC Number:
207-397-1
MDL number:
MFCD00001137
UNSPSC Code:
12352100
PubChem Substance ID:
24850882
NACRES:
NA.22

¥4,120

0 left in stock
Request a Bulk Order

Quality Level

100

Assay

96%

mp

162-166 °C (lit.)

functional group

carboxylic acid
hydroxyl

SMILES string

OC(=O)C1(O)c2ccccc2-c3ccccc13

InChI

1S/C14H10O3/c15-13(16)14(17)11-7-3-1-5-9(11)10-6-2-4-8-12(10)14/h1-8,17H,(H,15,16)

InChI key

GXAMYUGOODKVRM-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

9-Hydroxy-9-fluorenecarboxylic acid was used in the synthesis of a hexameric organooxotin prismane[1].

Pictograms

Environment
GHS09

Hazard Statements

H411

Precautionary Statements

P273

Hazard Classifications

Aquatic Chronic 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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.

JAN Code

180637-25G:
180637-5G:
180637-BULK:
180637-100G:
180637-VAR:

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCK5647
MKCQ9761
MKCL9529
MKCD8798
MKBR4320V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Vadapalli Chandrasekhar et al.
Journal of the American Chemical Society, 127(33), 11556-11557 (2005-08-18)
A hydroxyl-rich hexameric organooxotin prismane has been prepared by reaction of n-BuSn(O)OH with 9-hydroxy-9-fluorenecarboxylic acid. The supramolecular structure of this cage shows channels with hydrophobic and hydrophilic segments, which selectively entrap guest molecules.
Yusuke Nakajima et al.
Journal of experimental botany, 68(13), 3441-3456 (2017-06-22)
The direction of auxin transport changes in gravistimulated roots, causing auxin accumulation in the lower side of horizontally reoriented roots. This study found that auxin was similarly involved in hydrotropism and gravitropism in rice and pea roots, but hydrotropism in

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service