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1173883-99-2

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1173883-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1173883-99-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,3,8,8 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1173883-99:
(9*1)+(8*1)+(7*7)+(6*3)+(5*8)+(4*8)+(3*3)+(2*9)+(1*9)=192
192 % 10 = 2
So 1173883-99-2 is a valid CAS Registry Number.

1173883-99-2Downstream Products

1173883-99-2Relevant articles and documents

Pyridinium tribromide catalyzed condensation of indoles and aldehydes to form bisindolylalkanes

Yang, Qin,Yin, Zheng Lan,Ouyang, Ban Lai,Peng, Yi Yuan

, p. 515 - 518 (2011)

An efficient synthetic method for bis(indol-3-yl)alkane derivatives has been developed. In the presence of 5 mol% of pyridinium tribromide (PTB), the condensation of indoles and aldehydes proceeded smoothly under mild conditions, giving rise to the corresponding bis(indol-3-yl)alkanes in good to excellent yields.

Nitro-substituted 3,3′-bis(indolyl)methane-modified silica gel as a sorbent for solid-phase extraction of flavonoids

Wang, Na,Liang, Xiaojing,Li, Qian,Liao, Yuan,Shao, Shijun

, p. 15500 - 15506 (2015)

A novel solid-phase extraction (SPE) sorbent was synthesized by chemical immobilization of nitro-substituted 3,3′-bis(indolyl)methane onto pure silica. The nitro-substituted 3,3′-bis(indolyl)methane-modified silica was evaluated by elemental analysis (EA) and Fourier transform infrared spectroscopy (FT-IR). Coupled to high performance liquid chromatography (HPLC), the extraction performance of the sorbent was evaluated by using five flavonoids as model analytes. The results showed that the new sorbent could offer multiple intermolecular interactions, such as π-π, hydrophobic, and hydrogen bonding interactions. Several factors including the extraction material, sample solution pH, sample loading rate, eluent type, volume of eluent, elution rate, and volume of sample loading were optimized. Under the optimal conditions, the proposed method was applied for the analysis of five flavonoids in grape juice. Satisfactory linear ranges for flavonoids were obtained in the range of 10-200 ng mL-1 for myricetin, 5-200 ng mL-1 for quercetin and apigenin, and 1-200 ng mL-1 for luteolin and kaempferol, with correlation coefficients (R) ranging from 0.9908 to 0.9996. Limits of detection (LODs) were in the range of 0.5-10 ng mL-1. The recovery values of spiked grape juice ranged from 91.5% to 120.7% with relative standard deviations (RSDs) less than 9.12% (n = 5). As a novel solid-phase extraction sorbent, the nitro-substituted 3,3′-modified silica exhibited a higher extraction efficiency towards the tested compounds than diol-modified silica.

Facile access to bis(indolyl)methanes by copper-catalysed alkylation of indoles using alcohols under air

Nguyen, Ngoc-Khanh,Tran, Duc Long,Hung, Tran Quang,Le, Tra My,Son, Nguyen Thi,Trinh, Quang Thang,Dang, Tuan Thanh,Langer, Peter

supporting information, (2021/03/15)

Bis(3-indolyl)methanes (BIM) are important and present in the structure of many alkaloid and bioactive compounds (anti-inflammatory, anticancer, antiobesity, antimicrobial, etc.). Herein, we have reported an air stable and convenient Cu(OAc)2 c

Sulfonated Tetraphenylethylene-Based Hypercrosslinked Polymer as a Heterogeneous Catalyst for the Synthesis of Symmetrical Triarylmethanes via a Dual C-C Bond-Cleaving Path

Kalita, Gitumoni,Deka, Namrata,Paul, Dipankar,Thapa, Loknath,Dutta, Gitish K.,Chatterjee, Paresh Nath

supporting information, p. 304 - 308 (2020/12/14)

A sulfonic acid functionalized tetraphenylethylene-based hypercrosslinked polymer (THP-SO 3H) with a well-developed porous network and accessible sulfonic acid sites was synthesized and characterized by different analytical techniques. The cata

A facile iron-catalyzed dual C-C bond cleavage: An approach towards triarylmethanes

Paul, Dipankar,Khatua, Snehadrinarayan,Chatterjee, Paresh Nath

supporting information, p. 10056 - 10065 (2019/07/03)

A facile iron-catalyzed dual C-C bond cleaving reaction involving 1,3-dicarbonyl units along with electron-rich and sterically bulky arenes as efficient carbon-based leaving groups has been developed. The scope of the dual C-C bond breaking reaction was s

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