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3-benzyl-9-methyl-3,9-diaza-spiro[5.5]undecane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13323-40-5

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13323-40-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13323-40-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,2 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13323-40:
(7*1)+(6*3)+(5*3)+(4*2)+(3*3)+(2*4)+(1*0)=65
65 % 10 = 5
So 13323-40-5 is a valid CAS Registry Number.

13323-40-5Downstream Products

13323-40-5Relevant academic research and scientific papers

Preparation method of 3-alkyl-3, 9-diazaspiro [5, 5] undecane

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Paragraph 0109; 0111; 0115, (2020/08/29)

The invention relates to a preparation method of 3-alkyl-3, 9-diazaspiro [5, 5] undecane. The preparation method comprises the following steps: a. reacting a compound I with cyanoacetate under the action of ammonia water and a catalyst to obtain a compoun

1,2-DIHYDRO-3H-PYRAZOLO[3,4-D]PYRIMIDIN-3-ONE DERIVATIVE AS WEE1 INHIBITOR

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Paragraph 0242-0244, (2019/12/09)

The present invention provides a 1,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one compound having an inhibitory effect on Wee 1, and includes an application of the compound in treating various types of tumors.

CEPHEM COMPOUND HAVING CATECHOL GROUP

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Paragraph 0248; 0252, (2013/03/26)

A compound of the formula: wherein X is -N=, -CH=, or the like; W is -CH2- or the like; U is -S- or the like; R1 and R2 are each independently hydrogen, halogen, optionally substituted lower alkyl, or the like; R3/su

Practical and divergent synthesis of 1- and 5-substituted 3,9-diazaspiro[5.5]undecanes and undecan-2-ones

Yang, Hanbiao,Lin, Xiao-Fa,Padilla, Fernando,Rotstein, David M.

scheme or table, p. 6371 - 6374 (2009/04/07)

A divergent synthesis of 1- and 5-substituted 3,9-diazaspiro[5.5]undecanes and undecan-2-ones is described, in which the key step is an efficient Michael addition of a lithium enolate to a tetrasubstituted olefin acceptor. A variety of substituents (butyl, phenyl, and propoxyl) were introduced at C-1(5) in this manner. In addition, an asymmetric synthesis of one member of this series was achieved using an Evans oxazolidinone chiral auxiliary reagent.

SPIROCYCLIC SULFONAMIDES AND RELATED COMPOUNDS

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Page/Page column 54, (2010/11/29)

Spirocyclic sulfonamides and related compounds of Formula 1 are provided : (Formula (I)): in which the variables are as described herein. Such compounds may be used to modulate bradykinin receptor activity in vivo or in vitro, and are particularly useful

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