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化驗
97%
形狀
liquid
折射率
n20/D 1.488 (lit.)
bp
62 °C/5 mmHg (lit.)
密度
1.537 g/mL at 25 °C (lit.)
儲存溫度
2-8°C
SMILES 字串
OCCCBr
InChI
1S/C3H7BrO/c4-2-1-3-5/h5H,1-3H2
InChI 密鑰
RQFUZUMFPRMVDX-UHFFFAOYSA-N
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一般說明
在胶束介质和阳离子或非离子表面活性剂微乳液中，研究了 3-溴-1-丙醇、苯酚和一系列取代苯酚的反应。
3-溴-1-丙醇是一种亲电子试剂，可在亲核取代反应和氧化还原聚合反应中作为底物。
3-溴-1-丙醇是一种亲电子试剂，可在亲核取代反应和氧化还原聚合反应中作为底物。
應用
3-溴-1-丙醇被用于合成对荧光卤素敏感的喹啉类染料和熔融盐聚合物 。它被用于通过季铵氨基酸环化合成手性、季铵脯氨酸 。
最近用作斯文氧化法合成绿色试剂的接枝剂
訊號詞
Danger
危險聲明
危險分類
Acute Tox. 4 Oral - Eye Dam. 1
儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
149.0 °F - closed cup
閃點（°C）
65 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
Fredrik Currie
Journal of colloid and interface science, 277(1), 230-234 (2004-07-28)
The reaction between 3-bromo-1-propanol and phenol and a series of phenols carrying substituents in 4-position was studied in micellar media and in microemulsions based on either a cationic or a nonionic surfactant. The reactivity and the yield were evaluated and
Takeo Kawabata et al.
Journal of the American Chemical Society, 128(48), 15394-15395 (2006-11-30)
An enantiodivergent asymmetric cyclization of N-Boc-N-omega-bromoalkyl-alpha-amino acid derivatives has been developed. With potassium amide bases in DMF, cyclization proceeds with retention of configuration, while inversion of configuration was observed with lithium amide bases in THF. Chirality of the parent amino
Wei Song et al.
Molecules (Basel, Switzerland), 25(17) (2020-08-23)
Azobenzene (AB) units were successfully introduced into poly(1,6-heptadiyne)s in order to ensure smooth synthesis of double- and single-stranded poly(1,6-heptadiyne)s (P1 and P2) and simultaneously realize the self-assembly by Grubbs-III catalyst-mediated metathesis cyclopolymerization (CP) of AB-functionalized bis(1,6-heptadiyne) and 1,6-heptadiyne monomers (M1
Synthesis of molten salt-type polymer brush and effect of brush structure on the ionic conductivity.
Yoshizawa M and Ohno H.
Electrochimica Acta, 46(10), 1723-1728 (2001)
C D Geddes et al.
Analytical biochemistry, 293(1), 60-66 (2001-05-25)
Three fluorescent halide-sensitive quinolinium dyes have been produced by the reaction of the 6-methylquinoline heterocyclic nitrogen base with methyl bromide, methyl iodide, and 3-bromo-1-propanol. The quaternary salts, unlike the precursor molecule, are readily water soluble and the fluorescence intensity of
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