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methyl 3,5-bis(azidomethyl)benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

145665-38-9

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145665-38-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145665-38-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,6,6 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 145665-38:
(8*1)+(7*4)+(6*5)+(5*6)+(4*6)+(3*5)+(2*3)+(1*8)=149
149 % 10 = 9
So 145665-38-9 is a valid CAS Registry Number.

145665-38-9Relevant academic research and scientific papers

An efficient synthesis of an orthogonally protected aromatic diamine as scaffold for tweezer receptors with two different arms

Kuchelmeister, Hannes Y.,Schmuck, Carsten

experimental part, p. 4480 - 4485 (2009/12/25)

The synthesis of a new versatile template, 3-(N-Boc-aminomethyl)-5-(N-Fmoc- aminomethyl)benzoic acid (1), was developed and is hereby reported. The key feature of the synthetic strategy is the selective mono reduction of a symmetric diazide using a biphas

Solvent-induced amphiphilic molecular baskets: Unimolecular reversed micelles with different size, shape, and flexibility

Ryu, Eui-Hyun,Yan, Jie,Zhong, Zhenqi,Zhao, Yan

, p. 7205 - 7213 (2008/02/01)

Amphiphilic molecular baskets were obtained by attaching facially amphiphilic cholate groups to a covalent scaffold (calix[4]arene or 1,3,5-2,4,6-hexasubstituted benzene). In a solvent mixture consisting of mostly a nonpolar solvent (i.e., CCl4

Bivalent inhibitors of glutathione S-transferase: The effect of spacer length on isozyme selectivity

Maeda, Dean Y.,Mahajan, Sumit S.,Atkins, William M.,Zebala, John A.

, p. 3780 - 3783 (2007/10/03)

Glutathione S-transferases (GSTs) are cytosolic enzymes that catalyze the conjugation of glutathione with a variety of exogenous and endogenous electrophiles. High affinity, isozyme-specific inhibitors of GST are required for use as pharmacological tools

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