3-Penten-2-ol, predominantly trans - CAS 3899-34-1
Catalog: |
BB023818 |
Product Name: |
3-Penten-2-ol, predominantly trans |
CAS: |
3899-34-1 |
Synonyms: |
(E)-pent-3-en-2-ol |
IUPAC Name: | (E)-pent-3-en-2-ol |
Description: | 3-Penten-2-ol, predominantly trans (CAS# 3899-34-1 ) is a useful research chemical. |
Molecular Weight: | 86.13 |
Molecular Formula: | C5H10O |
Canonical SMILES: | CC=CC(C)O |
InChI: | InChI=1S/C5H10O/c1-3-4-5(2)6/h3-6H,1-2H3/b4-3+ |
InChI Key: | GJYMQFMQRRNLCY-ONEGZZNKSA-N |
Boiling Point: | 119-121 °C (lit.) |
Density: | 0.843 g/mL at 25 °C(lit.) |
Appearance: | Clear colorless liquid |
LogP: | 0.94330 |
Vapor Pressure: | 6.01 [mmHg] |
GHS Hazard Statement: | H226 (100%): Flammable liquid and vapor [Warning Flammable liquids] |
Precautionary Statement: | P210, P233, P240, P241, P242, P243, P280, P303+P361+P353, P370+P378, P403+P235, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
JP-WO2020017135-A1 | Ketone manufacturing method | 20180718 |
EP-3305839-A1 | Method for recycling polyolefin containing waste | 20161010 |
EP-3523366-A1 | Method for recycling polyolefin containing waste | 20161010 |
JP-2019531212-A | Recycling waste containing polyolefin | 20161010 |
KR-20190069476-A | Methods for recycling waste containing polyolefins | 20161010 |
PMID | Publication Date | Title | Journal |
12590492 | 20030226 | Volatile components and aroma active compounds in aqueous essence and fresh pink guava fruit puree (Psidium guajava L.) by GC-MS and multidimensional GC/GC-O | Journal of agricultural and food chemistry |
12207479 | 20020911 | Aroma active components in aqueous kiwi fruit essence and kiwi fruit puree by GC-MS and multidimensional GC/GC-O | Journal of agricultural and food chemistry |
11879031 | 20020313 | Characterization of the aromatic profile in aqueous essence and fruit juice of yellow passion fruit (Passiflora edulis Sims F. Flavicarpa degner) by GC-MS and GC/O | Journal of agricultural and food chemistry |
11871869 | 20020308 | A density-functional study of the mechanism for the diastereoselective epoxidation of chiral allylic alcohols by the titanium peroxy complexes | The Journal of organic chemistry |
Complexity: | 47.9 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 1 |
Exact Mass: | 86.073164938 |
Formal Charge: | 0 |
Heavy Atom Count: | 6 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 86.073164938 |
Rotatable Bond Count: | 1 |
Topological Polar Surface Area: | 20.2 Å2 |
Undefined Atom Stereocenter Count: | 1 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 0.8 |
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Alkenes
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS