Trans-2-Hexen-1-Ol

• CAS: 928-95-0
• Catalog Number: ACM928950
• Category: Alkenes
• Molecular Weight: 100.16
• Molecular Formula: C6H12O
• SMILES: CCC/C=C/CO
• Boiling Point: 158-160 °C
• Flash Point: 54°C
• Density: 0.844
• Solubility: water, 1.6e+004 mg/L @ 25 °C (est)
• Appearance: Colorless liquid
• Assay: 0.9999
• EC Number: 213-191-2
• Hazard Statements: H226
• MDL Number: MFCD00002927
• Packaging: 1 kg
• Refractive Index: 1.435-1.441
• RIDADR: UN 1993C 3 / PGIII
• Stability: Stable. Flammable. Incompatible with strong oxidizing agents, strong acids.
• Storage Conditions: Flammables area
• Symbol: GHS02

Custom Q&A

What is the molecular formula of trans-2-Hexen-1-ol?

The molecular formula of trans-2-Hexen-1-ol is C6H12O.

What is the molecular weight of trans-2-Hexen-1-ol?

The molecular weight of trans-2-Hexen-1-ol is 100.16 g/mol.

Is trans-2-Hexen-1-ol a natural product?

Yes, trans-2-Hexen-1-ol is a natural product found in Vitis rotundifolia, Psidium guajava, and other organisms.

What is the IUPAC name of trans-2-Hexen-1-ol?

The IUPAC name of trans-2-Hexen-1-ol is (E)-hex-2-en-1-ol.

What is the InChIKey of trans-2-Hexen-1-ol?

The InChIKey of trans-2-Hexen-1-ol is ZCHHRLHTBGRGOT-SNAWJCMRSA-N.

What are the synonyms of trans-2-Hexen-1-ol?

The synonyms of trans-2-Hexen-1-ol are (E)-Hex-2-en-1-ol and 2-HEXEN-1-OL.

What is the CAS number of trans-2-Hexen-1-ol?

The CAS number of trans-2-Hexen-1-ol is 928-95-0.

How many hydrogen bond donor counts does trans-2-Hexen-1-ol have?

Trans-2-Hexen-1-ol has one hydrogen bond donor count.

How many hydrogen bond acceptor counts does trans-2-Hexen-1-ol have?

Trans-2-Hexen-1-ol has one hydrogen bond acceptor count.

How many rotatable bond counts does trans-2-Hexen-1-ol have?

Trans-2-Hexen-1-ol has three rotatable bond counts.

Synthetic Use

Upstream Synthesis Route 1

• 6728-26-3

• 928-95-0

Reference: [1]Nakano, Tatsuya; Umano, Shigetoshi; Kino, Yoshio; Ishii, Yasutaka; Ogawa, Masaya
[Journal of Organic Chemistry, 1988, vol. 53, # 16, p. 3752 - 3757]

Upstream Synthesis Route 2

• 27829-72-7

• 928-95-0

Reference: [1]Bioorganic and Medicinal Chemistry Letters,2009,vol. 19,p. 5915 - 5918
[2]Chemistry of Natural Compounds,2000,vol. 36,p. 623 - 624
[3]Hoppe-Seyler's Zeitschrift fur Physiologische Chemie,1957,vol. 308,p. 277,282
[4]Chemistry - A European Journal,2012,vol. 18,p. 11880 - 11883

Downstream Synthesis Route 1

• 928-95-0

• 73881-10-4

Reference: [1]Gomez; Gellibert; Wagner; Mioskowski
[Tetrahedron Letters, 2000, vol. 41, # 32, p. 6049 - 6052]

* For details of the synthesis route, please refer to the original source to ensure accuracy.