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440094

Sigma-Aldrich

5-Chloro-2-fluorotoluene

98%

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About This Item

Linear Formula:
CH3C6H3(Cl)F
CAS Number:
452-66-4
Molecular Weight:
144.57
EC Number:
207-204-0
MDL number:
MFCD00018504
UNSPSC Code:
12352100
PubChem Substance ID:
24867565

Assay

98%

refractive index

n20/D 1.4995 (lit.)

bp

157-159 °C/752 mmHg (lit.)

density

1.188 g/mL at 25 °C (lit.)

SMILES string

Cc1cc(Cl)ccc1F

InChI

1S/C7H6ClF/c1-5-4-6(8)2-3-7(5)9/h2-4H,1H3

InChI key

JOXXHDGUTVUBDL-UHFFFAOYSA-N

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Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Warning

Hazard Statements

H226,H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

120.2 °F - closed cup

Flash Point(C)

49 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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K L Shepard et al.
Journal of medicinal chemistry, 34(10), 3098-3105 (1991-10-01)
For several decades a tantalizing goal for the treatment of primary open-angle glaucoma has been the development of a topically active carbonic anhydrase inhibitor. Recent results from several research groups indicate that considerable progress has been made toward this objective.
Dorus Heijnen et al.
Organic letters, 17(9), 2262-2265 (2015-04-15)
The palladium-catalyzed direct cross-coupling of a range of organic chlorides and bromides with the bifunctional C(sp(3))-(trimethylsilyl)methyllithium reagent is reported. The use of Pd-PEPPSI-IPent as the catalyst allows for the preparation of structurally diverse and synthetically versatile benzyl- and allylsilanes in
H Kanno et al.
Chemical & pharmaceutical bulletin, 40(8), 2049-2054 (1992-08-01)
New 1,4-dihydropyridine derivatives bearing a 4-(disubstituted phenyl) ring and an aminoethyl ester or an amino-2,2-dimethyl-propyl ester were synthesized and their antihypertensive activities were examined in normotensive rats and spontaneously hypertensive rats. The effects of phenyl substituents and ester groups on

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