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Benzamide, N,N'-[1,6-hexanediylbis(iminocarbonothioyl)]bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

7710-09-0

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7710-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7710-09-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,1 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7710-09:
(6*7)+(5*7)+(4*1)+(3*0)+(2*0)+(1*9)=90
90 % 10 = 0
So 7710-09-0 is a valid CAS Registry Number.

7710-09-0Downstream Products

7710-09-0Relevant articles and documents

Antituberculosis and antifungal activities of synthesized benzoylthiourea derivatives

Zhao, Meng-Meng,Dong, Xiu-Yan,Li, Gang,Yang, Yu-Hua,Zhang, Yu-Jie,Yang, Xiao-Qin

, p. 7551 - 7553 (2013)

A series of benzoylthiourea derivatives have been synthesized from benzoyl isothiocyanate and phenyleneamine in CH2Cl2 medium under solid-liquid phase transfer catalysis conditions. Structures of these compounds have been characteriz

Antibacterial guanidine oligomer with resistance to drug resistance, and preparation method and application thereof

-

Paragraph 0083-0084, (2021/09/04)

The invention discloses an antibacterial guanidine oligomer with resistance to drug resistance, a preparation method of the antibacterial guanidine oligomer, and application of the antibacterial guanidine oligomer in the field of materials. The antibacter

Structure-Activity Relationship of Hetarylpropylguanidines Aiming at the Development of Selective Histamine Receptor Ligands?

Pockes, Steffen,Wifling, David,Buschauer, Armin,Elz, Sigurd

, p. 285 - 297 (2019/04/04)

New classes of alkylated hetarylpropylguanidines with different functionality and variation in spacer length were synthesized to determine their behavior at the four histamine receptor (H1R, H2R, H3R, H4R) subtypes. Alkylated guanidines with different terminal functional groups and varied basicity, like amine, guanidine and urea were developed, based on the lead structure SK&F 91486 (2). Furthermore, heteroatomic exchange at the guanidine structure of 2 led to simple analogues of the lead compound. Radioassays at all histamine receptor subtypes were accomplished, as well as organ bath studies at the guinea pig (gp) ileum (gpH1R) and right atrium (gpH2R). Ligands with terminal functionalization led to, partially, highly affine and potent structures (two digit nanomolar), which showed up a bad selectivity profile within the histamine receptor family. While the benzoylurea derivative 144 demonstrated a preference towards the human (h) H3R, S-methylisothiourea analogue 143 obtained high affinity at the hH4R (pKi=8.14) with moderate selectivity. The molecular basis of the latter finding was supported by computational studies.

An efficient synthesis of polymethylene-bis-aroyl thiourea derivatives under the condition of phase-transfer catalysis

Zhang, You-Ming,Wei, Tai-Bao,Xian, Liang,Gao, Li-Ming

, p. 2007 - 2013 (2007/10/03)

Reaction of polymethylene diamine with aroyl chloride and ammonium thiocyanate under the condition of solid-liquid phase-transfer catalysis using polyethylene glycol-400 (PEG-400) as the catalyst yielded polymethylene-bis- aroyl thiourea derivatives 3a-q

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