W213209
Benzoin
≥98%
동의어(들):
α-Hydroxy-α-phenylacetophenone, α-Hydroxybenzyl phenyl ketone, 2-Hydroxy-2-phenylacetophenone
로그인조직 및 계약 가격 보기
모든 사진(1)
About This Item
Linear Formula:
C6H5CH(OH)COC6H5
CAS Number:
Molecular Weight:
212.24
FEMA Number:
2132
Beilstein:
391839
EC Number:
유럽평의회 번호:
162
MDL number:
UNSPSC 코드:
12164502
PubChem Substance ID:
플래비스(Flavis) 번호:
7.028
생물학적 소스
synthetic
Grade
Kosher
규정 준수
FDA 21 CFR 172.515
FDA 21 CFR 73.1
분석
≥98%
bp
194 °C/12 mmHg (lit.)
mp
134-138 °C (lit.)
응용 분야
flavors and fragrances
감각 수용성의
medicinal; vanilla; balsamic
SMILES string
OC(c1ccccc1)C(=O)c2ccccc2
InChI
1S/C14H12O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13,15H
InChI key
ISAOCJYIOMOJEB-UHFFFAOYSA-N
유전자 정보
human ... ACHE(43) , BCHE(590) , CES1(1066)
유사한 제품을 찾으십니까? 방문 제품 비교 안내
기타 정보
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Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
Sarvesh Kumar et al.
Archiv der Pharmazie, 345(5), 368-377 (2011-12-23)
The interaction between leukocytes and the vascular endothelial cells (EC) via cellular adhesion molecules plays an important role in the pathogenesis of various inflammatory and autoimmune diseases. Small molecules that block these interactions have been targeted as potential therapeutic agents
Direct copper-catalyzed α-arylation of benzyl phenyl ketones with aryl iodides: route towards tamoxifen.
Grégory Danoun et al.
Angewandte Chemie (International ed. in English), 51(51), 12815-12819 (2012-11-13)
Jun He et al.
Electrophoresis, 32(10), 1164-1175 (2011-04-19)
In the present work we report, for the first time, the successful on-line coupling of chiral MEKC (CMEKC) to atmospheric pressure photoionization MS (APPI-MS). Four structurally similar neutral test solutes (e.g. benzoin (BNZ) derivatives) were successfully ionized by APPI-MS. The
Yankai Liu et al.
Organic letters, 14(5), 1310-1313 (2012-03-03)
Expanding upon the recently developed aminocatalytic asymmetric indole-2,3-quinodimethane strategy, a straightforward synthesis of structurally and stereochemically complex tetrahydrocarbazoles has been devised. The chemistry's complexity-generating power was further harnessed by designing a multicatalytic, one-pot Diels-Alder/benzoin reaction sequence to stereoselectively access trans-fused
Total synthesis and absolute stereochemistry of seragakinone A.
Akiomi Takada et al.
Angewandte Chemie (International ed. in English), 50(10), 2297-2301 (2011-02-26)
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