103-30-0
103-30-0
Chemical Structure
trans-Stilbene
Synonym(s): (E)-Stilbene
- CAS No.: 103-30-0
- Formula:C14H12
- Molecular Weight:180.25
IUPAC Name: (E)-1,2-diphenylethene
InChIKey: PJANXHGTPQOBST-VAWYXSNFSA-N
SMILES: C1(/C=C/C2=CC=CC=C2)=CC=CC=C1
Biological Activity: trans-Stilbene ((E)-Stilbene) is used in the manufacturing of dye lasers, optical brighteners, non-steroidal synthetic estrogens[1].
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trans-Stilbene | 99.98% | trans-Stilbene ((E)-Stilbene) is used in the manufacturing of dye lasers, optical brighteners, non-steroidal synthetic estrogens. | ||||||||||||||||||||
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trans-Stilbene-d10 | trans-Stilbene-d10 ((E)-Stilbene-d10) is the deuterium labeled trans-Stilbene (HY-128793). trans-Stilbene ((E)-Stilbene) is used in the manufacturing of dye lasers, optical brighteners, non-steroidal synthetic estrogens. | |||||||||||||||||||||
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trans-Stilbene-d12 | trans-Stilbene-d12 ((E)-Stilbene-d12) is the deuterium labeled trans-Stilbene (HY-128793). trans-Stilbene ((E)-Stilbene) is used in the manufacturing of dye lasers, optical brighteners, non-steroidal synthetic estrogens. | |||||||||||||||||||||
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trans-Stilbene-d2 | trans-Stilbene-d2 ((E)-Stilbene-d2) is the deuterium labeled trans-Stilbene (HY-128793). trans-Stilbene ((E)-Stilbene) is used in the manufacturing of dye lasers, optical brighteners, non-steroidal synthetic estrogens. | |||||||||||||||||||||
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trans-Stilbene-13C2 | trans-Stilbene-13C2 ((E)-Stilbene-13C2) is the 13C labeled trans-Stilbene (HY-128793). trans-Stilbene ((E)-Stilbene) is used in the manufacturing of dye lasers, optical brighteners, non-steroidal synthetic estrogens. | |||||||||||||||||||||
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(E/Z)-SIB-1893 | 99.80% | (E/Z)-SIB-1893 is a racemic compound of (E)-SIB-1893 and (Z)-SIB-1893 isomers. (E)-SIB-1893 is a selective non-competitive metabotropic glutamate subtype 5 receptor (mGluR5) antagonist. | ||||||||||||||||||||
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SIB-1893 | SIB-1893 is an active compound. | |||||||||||||||||||||
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(E)-4-Stilbenol | (E)-4-Stilbenol is a hydroxylated stilbene compound and also a fungicide. (E)-4-Stilbenol inhibits the growth of Gloeophyllum trabeum and Poria placenta. (E)-4-Stilbenol is applicable to research related to fungal infections. | |||||||||||||||||||||
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Bibenzyl | 99.97% | Bibenzyl (s-Diphenylethane; Dibenzyl) is the parent core structure of bibenzyl-type natural products and an intermediate in organic synthesis. Hydroxyl-substituted derivatives of Bibenzyl are mainly isolated from plants such as Dendrobium (Orchidaceae) and Cannabaceae. These derivatives accumulate when plants are exposed to fungal infection and biotic stress, and exhibit antioxidant, anti-inflammatory, and anti-hepatic steatosis activities. | ||||||||||||||||||||
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Benzhydrol | 99.96% | Diphenylmethanol is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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Diphenylmethane | 99.99% | Diphenylmethane (Benzylphenyl) is an aromatic compound used as a drug intermediate. Diphenylmethane in the fragrance industry is used as an oxidizing agent and in soaps; in pesticides, as a synergist; and in dyes, as a plasticizer. | ||||||||||||||||||||
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Diphenylmethane-d2 | Diphenylmethane-d2 (Benzylphenyl-d2) is the deuterium labeled Diphenylmethane (HY-W008814). Diphenylmethane (Benzylphenyl) is an aromatic compound used as a drug intermediate. Diphenylmethane in the fragrance industry is used as an oxidizing agent and in soaps; in pesticides, as a synergist; and in dyes, as a plasticizer. | |||||||||||||||||||||
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4-(2-Phenylethenyl)pyridine | 4-(2-Phenylethenyl)pyridine is a metal-organic framework (MOF). | |||||||||||||||||||||
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Benzophenone-13C | 99.80% | Benzophenone-13C is the 13C labeled Benzophenone (HY-Y0546). Benzophenone is an endogenous metabolite. Benzophenone is a photosensitizer, that absorbs UV light, transfers its energy to DNA, and triggers DNA damage. Benzophenone can be used as the fragrance enhancer, ultraviolet curing agent, additive in plastics, or the flavor ingredient. Benzophenone can also be used in the manufacturing of insecticides, agricultural chemicals, hypnotics, antihistamines, and other pharmaceuticals. Benzophenone exhibits certain carcinogenicity in mouse/rat models under long term exposure. Benzophenone exhibits estrogenic activity. | ||||||||||||||||||||
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