Home Cart 0 Sign in  
X

[ CAS No. 619-38-5 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
3d Animation Molecule Structure of 619-38-5
Chemical Structure| 619-38-5
Chemical Structure| 619-38-5
Structure of 619-38-5 * Storage: {[proInfo.prStorage]}
Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Search after Editing

* Storage: {[proInfo.prStorage]}

* Shipping: {[proInfo.prShipping]}

Quality Control of [ 619-38-5 ]

Related Doc. of [ 619-38-5 ]

Alternatived Products of [ 619-38-5 ]
Product Citations

Product Details of [ 619-38-5 ]

CAS No. :619-38-5 MDL No. :
Formula : C16H32O2 Boiling Point : -
Linear Structure Formula :- InChI Key :QMTHILFALDMACK-UHFFFAOYSA-N
M.W : 256.42 Pubchem ID :222518
Synonyms :

Safety of [ 619-38-5 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362-P403+P233-P405-P501 UN#:
Hazard Statements:H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 619-38-5 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 619-38-5 ]

[ 619-38-5 ] Synthesis Path-Downstream   1~14

  • 1
  • [ 64-17-5 ]
  • [ 619-38-5 ]
  • [ 63905-75-9 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; calcium chloride
  • 2
  • [ 5277-39-4 ]
  • [ 619-38-5 ]
YieldReaction ConditionsOperation in experiment
With hydrogen bromide at 160℃;
  • 3
  • [ 619-38-5 ]
  • [ 408539-21-9 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride
  • 4
  • [ 619-38-5 ]
  • 2-bromo-2-heptyl-nonanoic acid ethyl ester [ No CAS ]
YieldReaction ConditionsOperation in experiment
With phosphorus; bromine anschliessend Behandeln mit Alkohol;
  • 5
  • [ 619-38-5 ]
  • [ 56-81-5 ]
  • 1,2,3-tris-(2-heptyl-nonanoyloxy)-propane [ No CAS ]
YieldReaction ConditionsOperation in experiment
at 225 - 235℃;
  • 6
  • [ 619-38-5 ]
  • [ 100-51-6 ]
  • 2-heptyl-nonanoic acid benzyl ester [ No CAS ]
YieldReaction ConditionsOperation in experiment
With zinc at 210℃;
YieldReaction ConditionsOperation in experiment
With potassium hydroxide
YieldReaction ConditionsOperation in experiment
Erhitzen ueber den Schmelzpunkt;
  • 9
  • 2,2-diheptyl-acetoacetic acid ethyl ester [ No CAS ]
  • [ 64-17-5 ]
  • [ 619-38-5 ]
  • [ 64-19-7 ]
  • 10
  • [ 71195-62-5 ]
  • [ 619-38-5 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: aqueous ethanol 2: aqueous hydrobromic acid / 160 °C
  • 11
  • [ 1653-35-6 ]
  • [ 619-38-5 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: phosphorus; iodine / 140 °C 2: aqueous ethanol 3: aqueous hydrobromic acid / 160 °C
  • 12
  • [ 619-38-5 ]
  • [ 120138-90-1 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: thionyl chloride 2: palladium/barium sulfate; xylene / 140 °C / Hydrogenation.mit Chinolin und Schwefel desaktiviertem Katalysator
  • 13
  • [ 619-38-5 ]
  • 2-heptyl-nonanal semicarbazone [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: thionyl chloride 2: palladium/barium sulfate; xylene / 140 °C / Hydrogenation.mit Chinolin und Schwefel desaktiviertem Katalysator
YieldReaction ConditionsOperation in experiment
In currently preferred embodiments, the useful compounds are selected from the group consisting of: 2-Pentylheptanoic acid [M (5,5)], 2-Propyldodecanoic acid [M (3,10)], 2-Propylnonanoic acid [M (3,7)], 2-Heptylnonanoic acid [M (7,7)], 1-O-stearoyl-2-propylnonayl-sn-glycero-3-phosphatidylcholine [DP-M(3,7)], 1-O-stearoyl-2-pentylheptonayl-sn-glycero-3-phosphatidylcholine [DP-M (5,5)], 1-O-stearoyl-2-heptylnonayl-sn-glycero-3-phosphatidylcholine [DP-M (7,7)], and 1-O-stearoyl-2-propyldodecanoyl-sn-glycero-3-phosphatidylcholine [DP-M (3,10)].
, wherein said compound of the general formula I is selected from the group consisting of: 2-Pentylheptanoic acid; 2-Propyldodecanoic acid, 2-Propylnonanoic acid, and 2-Heptylnonanoic acid.
In currently preferred embodiments, the useful compounds are selected from the group consisting of: 2-Pentylheptanoic acid [M (5,5)], 2-Propyldodecanoic acid [M (3,10)], 2-Propylnonanoic acid [M (3,7)], 2-Heptylnonanoic acid [M (7,7)], 1-stearoyl-2-propylnonanoyl-sn-glycero-3-phosphocholine, 1-stearoyl-2-pentylheptanoyl-sn-glycero-3-phosphocholine, 1-stearoyl-2-heptylnonanoyl-sn-glycero-3-phosphocholine, and 1-stearoyl-2-propyldodecanoyl-sn-glycero-3-phosphocholine.
The method according to claim 1, wherein said compound of the general formula I is selected from the group consisting of: 2-Pentylheptanoic acid; 2-Propyldodecanoic acid, 2-Propylnonanoic acid, and 2-Heptylnonanoic acid.
In a currently preferred embodiment, the compound of the general formula I is selected from the group consisting of: ... 2-propyldodecanoic acid, 2-propyltetradecanoic acid, 2-propyloctadecanoic acid, 2-propyleicosanoic acid, 2-heptylnonanoic acid, 2-heptyldodecanoic acid, 2-decyldodecanoic acid, 2-decylhexadecanoic acid, ...
The method according to claim 1, wherein said compound of the general formula I is selected from the group consisting of: ... 2-propyltetradecanoic acid, 2-propylhexadecanoic acid, 2-propyloctadecanoic acid, 2-propyleicosanoic acid, 2-heptylnonanoic acid, 2-heptyldodecanoic acid, 2-heptylhexadecanoic acid, 2-decyldodecanoic acid, ...

Recommend Products
Same Skeleton Products
Historical Records