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560855

Sigma-Aldrich

10-溴-1-癸烯

97%

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5 G
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5 G
$337.00

About This Item

线性分子式:
Br(CH2)8CH=CH2
CAS号:
62871-09-4
分子量:
219.16
MDL號碼:
MFCD00078660
分類程式碼代碼:
12352100
PubChem物質ID:
24879896
NACRES:
NA.22

$337.00

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品質等級

100

化驗

97%

折射率

n20/D 1.4660 (lit.)

bp

50 °C/0.3 mmHg (lit.)

密度

1.092 g/mL at 25 °C (lit.)

官能基

alkyl halide
allyl
bromo

SMILES 字串

BrCCCCCCCCC=C

InChI

1S/C10H19Br/c1-2-3-4-5-6-7-8-9-10-11/h2H,1,3-10H2

InChI 密鑰

JVVPJOMYWVYPOF-UHFFFAOYSA-N

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相关类别

一般說明

10-Bromo-1-decene can be synthesized by reacting 9-decen-1-ol with PBr3.[1] The product undergoes reduction reaction with 2-propylbenzo[d][1,3,2]dioxaborole (PBD) and Bu3SnH under room temperature conditions to yield 1-decene.[2]

包裝

10-Bromo-1-decene may be used to synthesize:
  • 4′-(9-decenyloxy) biphenyl-4-carboxylic acid methyl ester[3]
  • 4′-(9-decenyloxy)biphenyl-4-carboxylic acid[4]
  • 9-decenylmagnesium bromide, which was employed for the preparation of (R)-tridec-12-en-2-ol[5]

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H315,H319,H335

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

206.0 °F - closed cup

閃點（°C）

96.67 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKCN5841
MKCB9344
MKBZ8263V
MKBW2535V
MKBR6624V

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A simple access to gamma,delta-unsaturated-beta-keto lactones is presented, allowing a rapid total synthesis of the naturally occurring 16-membered macrolide antibiotic (-)-A26771B via cross metathesis, asymmetric dihydroxylation, and lactonization as the key steps.
The four-membered-ring chemical shift anomaly.
Lambert JB, et al.
The Journal of Organic Chemistry, 48(22), 3982-3985 (1983)
Room temperature ferroelectric terpolymers with large spontaneous polarization.
Naciri J, et al.
Macromolecules, 28(15), 5274-5279 (1995)
Novel ferroelectric and electroclinic organosiloxane liquid crystals.
Naciri J, et al.
Chemistry of Materials, 7(7), 1397-1402 (1995)
Radical initiation using borole derivatives.
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Tetrahedron Letters, 49(4), 628-630 (2008)

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