P78
棕榈酰氯
98%
别名:
十六酰氯
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关于此项目
线性分子式:
CH3(CH2)14COCl
化学文摘社编号:
分子量:
274.87
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-996-7
Beilstein/REAXYS Number:
972409
MDL number:
Assay:
98%
产品名称
棕榈酰氯, 98%
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
SMILES string
CCCCCCCCCCCCCCCC(Cl)=O
assay
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.)
Quality Level
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Application
棕榈酰氯可用于：
也可用于全合成以下物质：
- 通过立体选择性烯烃交叉复分解，将碳链引入糖鞘脂半乳糖神经酰胺。
- 通过环氧乙烷的区域选择性开环,制备单酰基和1,3-对称的三酰基甘油。
也可用于全合成以下物质：
- 猴头菌酮J(Hericenone J)和5′ -脱氧代猴头菌酮 C（hericene A）。
- 甘露糖脂。
- 分枝杆菌素S和分枝杆菌素T等同物，其具有儿茶酚-甘氨酸基团而非天然存在分枝杆菌素所含的酚-恶唑啉基团。
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
supp_hazards
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
320.0 °F - closed cup
flash_point_c
160 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Kyoung-Hwa Choi et al.
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
Rapid access to 6-bromo-5, 7-dihydroxyphthalide 5-methyl ether by a CuBr2-mediated multi-step reaction: concise total syntheses of hericenone J and 5′ -deoxohericenone C (hericene A)
Kobayashi S, et al.
Tetrahedron, 67(47), 9087-9092 (2011)
Takeshi Harayama et al.
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
Shimada N, et al.
Organic & Biomolecular Chemistry, 17(31), 7325-7329 (2019)
Synthesis and studies of catechol-containing mycobactin S and T analogs
Walz AJ, et al.
Organic & Biomolecular Chemistry, 5(10), 1621-1628 (2007)
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