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222054

Sigma-Aldrich

4-Heptylbenzoyl chloride

99%

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About This Item

Linear Formula:
CH3(CH2)6C6H4COCl
CAS Number:
50606-96-7
Molecular Weight:
238.75
EC Number:
256-648-1
MDL number:
MFCD00000702
UNSPSC Code:
12352100
PubChem Substance ID:
24853309
NACRES:
NA.22

Assay

99%

form

liquid

refractive index

n20/D 1.5218 (lit.)

density

1.002 g/mL at 25 °C (lit.)

functional group

acyl chloride

SMILES string

CCCCCCCc1ccc(cc1)C(Cl)=O

InChI

1S/C14H19ClO/c1-2-3-4-5-6-7-12-8-10-13(11-9-12)14(15)16/h8-11H,2-7H2,1H3

InChI key

WHTFLTOKFXTJGV-UHFFFAOYSA-N

Application

4-Heptylbenzoyl chloride was used in the synthesis of 3-O-acyl derivative by reacting with betulinic acid.

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H314,H335

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBL0237
STBK0729
STBH9944
STBG6479
STBF6624V

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Rama Mukherjee et al.
Bioorganic & medicinal chemistry letters, 14(12), 3169-3172 (2004-05-20)
New 3-O-acyl, 3-benzylidene, 3-hydrazone, 3-hydrazine, 17-carboxyacryloyl ester derivatives of betulinic acid (2-6, 8-11, 13, 17, 18, 21, and 22) were synthesized and evaluated in vitro for anti-angiogenic activity on endothelial cell cytotoxicity, specificity, and tube-formation ability. All derivatives reported here

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