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Key Documents

713732

Sigma-Aldrich

6-氨基-2-氰基苯并噻唑

97%

同義詞:

2-氰基-6-氨基苯并噻唑, 6-氨基-2-苯并噻唑甲腈

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About This Item

經驗公式(希爾表示法):
C8H5N3S
CAS號碼:
分子量::
175.21
Beilstein:
1567902
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

≥96.5% (HPLC)
97%

形狀

crystals

官能基

nitrile

儲存溫度

2-8°C

SMILES 字串

Nc1ccc2nc(sc2c1)C#N

InChI

1S/C8H5N3S/c9-4-8-11-6-2-1-5(10)3-7(6)12-8/h1-3H,10H2

InChI 密鑰

ZOHSEULTWOYIMS-UHFFFAOYSA-N

包裝

无底玻璃瓶。内含物在插入的融合锥体内。

象形圖

CorrosionExclamation mark

訊號詞

Danger

危險聲明

危險分類

Acute Tox. 4 Oral - Eye Dam. 1

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Stefano Menegatti et al.
Advanced healthcare materials, 4(15), 2297-2305 (2015-09-16)
Combinations of polymer conjugates affording in situ gelation hold promise for treatment of pathological cavities (e.g., arthritis) and sustained drug release. In particular, hyaluronic acid (HA) functionalized with reactive groups is regarded as an excellent biomaterial due to its tunable
Yuanyuan Yang et al.
Journal of biomedical nanotechnology, 14(8), 1396-1408 (2018-06-16)
Despite the great achievements of nanomedicines made in cancer chemotherapy, precise tumor targeting and deep penetration are still major challenges. Many nanomedicines can only passively accumulate near leaky site of tumor vessels through the enhanced permeability and retention (EPR) effect
Pavlo V Khodakivskyi et al.
Science advances, 7(6) (2021-02-05)
The microbiome-produced enzyme bile salt hydrolase (BSH) plays a central role in human health, but its function remains unclear due to the lack of suitable methods for measuring its activity. Here, we have developed a novel optical tool based on
Nitin A Patil et al.
Bioconjugate chemistry, 30(3), 793-799 (2019-01-16)
Antisense oligonucleotide (ASO)-based drugs are emerging with great potential as therapeutic compounds for diseases with unmet medical needs. However, for ASOs to be effective as clinical entities, they should reach their intracellular RNA and DNA targets at pharmacologically relevant concentrations.

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