추천 제품
Quality Level
분석
98%
refractive index
n20/D 1.452 (lit.)
bp
88-90 °C/0.2 mmHg (lit.)
mp
11-13 °C (lit.)
density
0.906 g/mL at 25 °C (lit.)
SMILES string
CCCCCCCCCCCCCCCC(Cl)=O
InChI
1S/C16H31ClO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18/h2-15H2,1H3
InChI key
ARBOVOVUTSQWSS-UHFFFAOYSA-N
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애플리케이션
Palmitoyl chloride can be used:
It can also be used in the total synthesis of:
- To introduce carbon chain in glycosphingolipid galactosyl ceramide through stereoselective olefin cross-metathesis.
- To prepare monoacyl and 1,3-symmetrical triacylglycerols via regioselective ring opening of an oxirane.
It can also be used in the total synthesis of:
- Hericenone J and 5′ -deoxohericenone C (hericene A).
- Seminolipid.
- Mycobactin S and T equivalents having catechol-glycine group instead of phenol-oxazoline of the naturally occurring mycobactins.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Skin Corr. 1B
보충제 위험성
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 1
Flash Point (°F)
320.0 °F - closed cup
Flash Point (°C)
160 °C - closed cup
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
이미 열람한 고객
Carbohydrate polymers, 246, 116487-116487 (2020-08-05)
The purpose of this study was to investigate the improvement in the hydrophobicity of cellulose through gas grafting treatment with long chain fatty acid chloride using high pressure during pressing at high temperature. To do this, the gas grafting treatment
Regioselective opening of an oxirane system with trifluoroacetic anhydride. A general method for the synthesis of 2-monoacyl-and 1, 3-symmetrical triacylglycerols
Tetrahedron, 61(15), 3659-3669 (2005)
Synthesis of the glycosphingolipid β-galactosyl ceramide and analogues via olefin cross metathesis
The Journal of Organic Chemistry, 70(20), 8228-8230 (2005)
Synthesis and studies of catechol-containing mycobactin S and T analogs
Organic & Biomolecular Chemistry, 5(10), 1621-1628 (2007)
The Journal of pharmacy and pharmacology, 69(9), 1110-1115 (2017-06-18)
Apomorphine is used to symptomatically treat Parkinson's disease (PD). Oral delivery of apomorphine is generally limited by its short plasma half-life and a hepatic first-pass metabolism. This study was aimed at evaluating the behavioural response of apomorphine and its prodrug
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