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22070

Supelco

(+)-香芹酮

analytical standard

别名:

(+)-p-薄荷-6,8-二烯 2-酮, (S)-5-异丙烯基-2-甲基-2-环已烯酮

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About This Item

经验公式（希尔记法）:
C10H14O
CAS号:
2244-16-8
分子量:
150.22
Beilstein:
2042970
EC號碼:
218-827-2
MDL號碼:
MFCD00062997
分類程式碼代碼:
85151701
PubChem物質ID:
329752243

等級

analytical standard

品質等級

100

化驗

≥98.5% (sum of enantiomers, GC)

光學活性

[α]20/D +61±2°, neat

儲存期限

limited shelf life, expiry date on the label

技術

HPLC: suitable
gas chromatography (GC): suitable

折射率

n20/D 1.499

bp

228-230 °C (lit.)

密度

0.960 g/mL at 20 °C (lit.)

應用

agriculture
environmental
food and beverages

格式

neat

SMILES 字串

CC(=C)[C@H]1CC=C(C)C(=O)C1

InChI

1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9H,1,5-6H2,2-3H3/t9-/m0/s1

InChI 密鑰

ULDHMXUKGWMISQ-VIFPVBQESA-N

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相关类别

一般說明

（+）-香芹酮（S-香芹酮）是一种单萜，具有影响植物生长发育和微生物活性调节的能力，它还可以通过抑制苯丙氨酸氨裂合酶（PAL）的诱导来防止马铃薯发芽。

應用

有关合适的仪器技术的更多信息，请参阅产品′的检验报告。想要获得更多支持，请联系技术服务部。

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H317

危險分類

Skin Sens. 1A

儲存類別代碼

10 - Combustible liquids

水污染物質分類（WGK）

WGK 1

閃點（°F）

204.1 °F - closed cup

閃點（°C）

95.6 °C - closed cup

個人防護裝備

Eyeshields, Gloves

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分析证书(COA)

Lot/Batch Number
BCCG0400
BCCC7860
BCCC4533
BCBZ8472
BCBZ3308

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Possible regulatory role of phenylalanine ammonia?lyase in the production of anthocyanins in asparagus (Asparagus officinalis L).
Flores, Francisco B., et al.
Journal of the Science of Food and Agriculture, 85.6, 925-930 (2005)
Raul Conde et al.
Phytomedicine : international journal of phytotherapy and phytopharmacology, 18(14), 1197-1201 (2011-08-02)
There is no universally accepted and effective prophylaxis of migraine headache episodes. Thus we aimed to investigate the effects of Lippia alba (Mill.) N. E. Brown, an herb with many effects on central nervous system, on pain frequency and intensity
Marta Goretti et al.
Bioresource technology, 121, 290-297 (2012-08-04)
Response surface methodology was applied in optimizing the asymmetric bioreduction of (4S)-(+)-carvone to dihydrocarvone (with low incidence of unsought side reactions) by using whole-cells of Cryptococcus gastricus. A factorial design (2(5)) including five independent variables was performed: X(1)=incubation time; X(2)=pH;
Philipp Klahn et al.
Organic letters, 14(5), 1250-1253 (2012-02-14)
The total synthesis of (+)-cyperolone, an eudesmane-derived sesquiterpenoid from Cyperus rotundus, is described. The de novo synthesis was accomplished via a 15 step sequence starting from (R)-(-)-carvone. The synthetic route features a platinum-catalyzed cycloisomerization to rapidly construct the bicyclic core
Elissavet E Anagnostaki et al.
Organic letters, 15(1), 152-155 (2012-12-22)
The synthesis of hydroxyelemane 5 from (R)-carvone and its utilization as a common synthetic scaffold to produce structurally diverse germacrane and guaiane sesquiterpenes are described. A highly enantio- and stereoselective biomimetic tandem oxy-Cope/ene rearrangement was used as the key reaction
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