| Identification | More | [Name]
1,1,3-Triphenylpropargyl alcohol | [CAS]
1522-13-0 | [Synonyms]
1,1,3-TRIPHENYL-2-PROPYN-1-OL
1,1,3-TRIPHENYL-PROP-2-YN-1-OL
1,1,3-TRIPHENYLPROPARGYL ALCOHOL
LABOTEST-BB LT00159755
RARECHEM AM UC 0715
TIMTEC-BB SBB009045
2-Propyn-1-ol, 1,1,3-triphenyl-
Benzenemethanol, alpha-phenyl-alpha-(phenylethynyl)- | [Molecular Formula]
C21H16O | [MDL Number]
MFCD00004449 | [Molecular Weight]
284.35 | [MOL File]
1522-13-0.mol |
| Chemical Properties | Back Directory | [Appearance]
Slightly yellow powder | [Melting point ]
80-82 °C (lit.) | [Boiling point ]
220 °C / 1mmHg | [density ]
1.18±0.1 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
Solid | [pka]
11.31±0.29(Predicted) | [color ]
White | [InChI]
1S/C21H16O/c22-21(19-12-6-2-7-13-19,20-14-8-3-9-15-20)17-16-18-10-4-1-5-11-18/h1-15,22H | [InChIKey]
VWRQCJRTHKUVNF-UHFFFAOYSA-N | [SMILES]
OC(C#Cc1ccccc1)(c2ccccc2)c3ccccc3 | [CAS DataBase Reference]
1522-13-0(CAS DataBase Reference) | [NIST Chemistry Reference]
Diphenyl(phenylethynyl)carbinol(1522-13-0) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S22:Do not breathe dust . | [WGK Germany ]
3
| [HS Code ]
29062900 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Acute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| Hazard Information | Back Directory | [Chemical Properties]
Slightly yellow powder | [Uses]
1,1,3-Triphenylpropargyl Alcohol is used as a reagent in the chemical synthesis of several organic compounds including that of polysubstituted 4H-thiopyrans from β-oxodithioesters and the one-pot synthesis of pyrazoles via a four-step cascade sequence. | [General Description]
1,1,3-Triphenylpropargyl alcohol can be used in the synthesis of a single isomer of a naphthalene compound. |
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