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
Journal of lipid research, 56(7), 1370-1379 (2015-05-30)
The surfactant proteins (SPs), SP-B and SP-C, are important components of pulmonary surfactant involved in the reduction of alveolar surface tension. Quantification of SP-B and SP-C in surfactant drugs is informative for their quality control and the evaluation of their
Total syntheses of seminolipid and its analogues by using 2, 6-bis (trifluoromethyl) phenylboronic acid as protective reagent
Organic & Biomolecular Chemistry, 17(31), 7325-7329 (2019)
Synthesis and studies of catechol-containing mycobactin S and T analogs
Organic & Biomolecular Chemistry, 5(10), 1621-1628 (2007)
Synthesis of the glycosphingolipid β-galactosyl ceramide and analogues via olefin cross metathesis
The Journal of Organic Chemistry, 70(20), 8228-8230 (2005)
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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