128007
1,5-二溴戊烷
97%
别名:
五亚甲基二溴
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关于此项目
线性分子式:
Br(CH2)5Br
化学文摘社编号:
分子量:
229.94
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-849-7
Beilstein/REAXYS Number:
1209245
MDL number:
Assay:
97%
Form:
liquid
InChI
1S/C5H10Br2/c6-4-2-1-3-5-7/h1-5H2
InChI key
IBODDUNKEPPBKW-UHFFFAOYSA-N
SMILES string
BrCCCCCBr
vapor density
8 (vs air)
assay
97%
form
liquid
Quality Level
refractive index
n20/D 1.512 (lit.)
bp
110 °C/15 mmHg (lit.)
mp
−34 °C (lit.)
density
1.688 g/mL at 25 °C (lit.)
functional group
bromo
General description
1,5-二溴戊烷是解脂耶氏酵母3589的一种生长补充剂。
Application
1,5-二溴戊烷可用于制备：
- 5-吡唑啉酮衍生物。
- O-烷基化间苯三酚衍生物，用于形成聚烷基芳基醚树枝状聚合物的中心核。
- 与1-甲基-7-甲氧基-2-四氢萘酮合成地佐辛中间体，即(R)-(+)-1-(5-溴戊基)-1-甲基-7-甲氧基-2-四氢萘酮。
1,5-二溴戊烷用于制备1,5-二-格氏试剂。它还用于合成新型螺环吡咯烷酮。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
174.2 °F - closed cup
flash_point_c
79 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Enantioselective phase-transfer catalyzed alkylation of 1-methyl-7-methoxy-2-tetralone: an effective route to dezocine
Li R, et al.
Beilstein Journal of Organic Chemistry, 14(1), 1421-1427 (2018)
Wieslaw M Kazmierski et al.
Bioorganic & medicinal chemistry letters, 12(23), 3431-3433 (2002-11-07)
We have developed concise and efficient syntheses of novel spirocyclic pyrrolidones 1-3, which involve the alkylation of pyrrolidone precursor 13 with 1,5-dibromopentane, 16 and 15, followed by an in situ lactamization. Conjugates of 1 and 2 with P1'/P2' hydroxy-indanolamine moiety
Aakanksha Vatsal et al.
Yeast (Chichester, England), 28(10), 721-732 (2011-09-10)
Yarrowia lipolytica 3589, a tropical marine yeast, grew aerobically on a broad range of bromoalkanes varying in carbon chain length and differing in degree and position of bromide group. Amongst the bromoalkanes studied, viz. 2-bromopropane (2-BP), 1-bromobutane (1-BB), 1,5-dibromopentane (1,5-DBP)
1, 5-Bis (4-dithiocarboxylate-5-hydroxypyrazolyl) pentane Derivatives of 5-Pyrazolones
Avila C, et al.
Journal of Heterocyclic Chemistry, 42(4), 595-597 (2005)
Synthesis of poly (alkyl aryl ether) dendrimers
Nithyanandhan J and Jayaraman N
The Journal of Organic Chemistry, 67(17), 6282-6285 (2002)
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