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アッセイ
98%
mp
>300 °C (lit.)
溶解性
water: soluble 1g/15ml, clear
SMILES記法
[Na]Sc1nnnn1-c2ccccc2
InChI
1S/C7H6N4S.Na/c12-7-8-9-10-11(7)6-4-2-1-3-5-6;/h1-5H,(H,8,10,12);/q;+1/p-1
InChI Key
RSZMKAPXKXEWBY-UHFFFAOYSA-M
詳細
1-Phenyl-1H-tetrazole-5-thiol sodium salt is a tetrazole derivative. The kinetics of its reaction with Diel′s-Alder adducts of 1,4-benzoquinone has been investigated.
シグナルワード
Warning
危険有害性情報
危険有害性の分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
ターゲットの組織
Respiratory system
保管分類コード
11 - Combustible Solids
WGK
WGK 3
引火点(°F)
Not applicable
引火点(℃)
Not applicable
個人用保護具 (PPE)
dust mask type N95 (US), Eyeshields, Gloves
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
423920-VAR:
423920-25G:
423920-5G:
423920-BULK:
Kinetics of the reaction of 1-phenyl-1H-tetrazole-5-thiol sodium salt with less substituted 1, 4-naphthoquinone 2, 3-epoxides.
The Journal of Organic Chemistry, 33(1), 262-265 (1968)
The Journal of organic chemistry, 73(7), 2527-2532 (2008-03-05)
In the presence of 1-phenyl-5-mercaptotetrazole as a nucleophile, electrochemical oxidations of 1,2- and 1,4-dihydroxybenzenes have been investigated in aqueous solution using cyclic voltammetry and controlled-potential coulometry. The voltammetric results indicate that an electrooxidative/Michael-type sequential reaction occurs between the mercaptide anion
Ceskoslovenska farmacie, 39(7), 294-298 (1990-09-01)
For the investigation of new anti-inflammatory drugs, 1-phenyl-5-mercaptotetrazole (I) was selected as the principal structure. The purpose itself lay in an alkylation of the mercapto group with different remainders. In some cases at the same time a substituent was introduced
Folia microbiologica, 45(2), 138-142 (2001-03-29)
The antifungal effect of substituted 1-phenyl-5-mercaptotetrazoles was tested with Candida tropicalis, C. pseudotropicalis, C. mogii, Trichosporon cutaneum, Cryptococcus albidus and S. cerevisiae. Candida strains exhibited the lowest sensitivity to the compounds; the most sensitive was S. cerevisiae. The MIC values
[Information from the Soviet Toxicology Center].
Gigiena truda i professional'nye zabolevaniia, (10)(10), 55-56 (1980-10-01)
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