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1H-Benzimidazole,1-(1-ethoxyethyl)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74586-44-0

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74586-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74586-44-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,5,8 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 74586-44:
(7*7)+(6*4)+(5*5)+(4*8)+(3*6)+(2*4)+(1*4)=160
160 % 10 = 0
So 74586-44-0 is a valid CAS Registry Number.

74586-44-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Dimethyl 7-{N-Ethyl-N-[4-(N-phthalimido)butyl]amino}naphthalene-1,2-dicarboxylate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:74586-44-0 SDS

74586-44-0Relevant academic research and scientific papers

(Diacetoxyiodo)benzene-Mediated Transition-Metal-Free Amination of C(sp3)-H Bonds Adjacent to Heteroatoms with Azoles: Synthesis of N-Alkylated Azoles

Sun, Bin,Yan, Zhiyang,Jin, Can,Su, Weike

supporting information, p. 2432 - 2436 (2018/11/23)

A novel PhI(OAc) 2 -mediated cross-dehydrogenative coupling reaction of α-C(sp 3)-H bonds adjacent to a hetero atom with various azoles has been developed, which provides an alternative method for constructing C-N bonds with high atom efficiency. This new protocol requires no metal catalyst and it provides ready access to a wide range of N-alkylated azole derivatives in moderate to excellent yields by using commercially available PhI(OAc) 2 as the sole oxidant. Furthermore, the method is effective on a gram scale, which highlights the practicality of this transformation. The result of radical-captured experiments indicated that the transformation might involve a free-radical pathway.

Cross-dehydrogenative coupling of azoles with α-c(sp3)-h of ethers and thioethers under metal-free conditions: Functionalization of h-n azoles via c-h activation

Aruri, Hariprasad,Singh, Umed,Sharma, Sumit,Gudup, Satish,Bhogal, Mukesh,Kumar, Sanjay,Singh, Deepika,Gupta, Vivek K.,Kant, Rajni,Vishwakarma, Ram A.,Singh, Parvinder Pal

, p. 1929 - 1936 (2015/02/19)

A metal-free cross-dehydrogenative coupling method for the synthesis of N-substituted azoles has been developed. The TBAI/TBHP system catalyzed the coupling of azoles with ethers and thioethers via α-C(sp3)-H activation. Under the optimized conditions, a diverse range of un/substituted azoles such as 1H-benzimidazole, 9H-purine, 1H-benzotriazole, 1H-1,2,3-triazole, 1H-1,2,4-triazole, and 1H-pyrazole were successfully employed for coupling with various ethers and thioethers such as tetrahydrofuran, tetrahydropyran, 1,4-dioxane, diethyl ether, tetrahydrothiophene, and 1,3-dithiolane.

Iron-catalyzed N -alkylation of azoles via oxidation of C-H bond adjacent to an oxygen atom

Pan, Shiguang,Liu, Jinhua,Li, Huanrong,Wang, Zhenyu,Guo, Xingwei,Li, Zhiping

supporting information; experimental part, p. 1932 - 1935 (2010/07/04)

Figure presented Azole derivatives were synthesized by iron-catalyzed oxidative reactions of azoles and ethers in good to excellent yields. A wide variety of azoles and ethers were selectively transformed into the corresponding oxidative coupling products under neutral reaction conditions.

REACTION OF 1-(1-ALKOXYALKYL)-1-H-1,2,4-TRIAZOLE WITH AMIDES

Ohta, Shunsaku,Maruyama, Akihiko,Kawasaki, Ikuo,Hatakeyama, Shoko,Ichikawa, Michiyo,Guro, Tomoko

, p. 2029 - 2036 (2007/10/02)

1-(1-Alkoxyalkyl)-1H-1,2,4-triazoles (4) were prepared by treating acetals (1) with 1H-1,2,4-triazole (2) in the presence of pyridinium p-toluenesulfonate (3).The alkoxy group of 4-was substituted with -NR4COR3 group by treating with carboxamides to give various 1-(1-acylaminoalkyl)-1H-1,2,4-triazole (6) in variable yields.

MECHANISMS FOR THE SOLVOLYTIC DECOMPOSITIONS OF NUCLEOSIDE ANALOGUES-I. ACIDIC HYDROLYSIS OF 2-SUBSTITUTED 1-(1-ETHOXYETHYL)BENZIMIDAZOLES

Loennberg, Harri,Kaeppi, Rainer

, p. 913 - 918 (2007/10/02)

A few 2-substituted 1-(1-ethoxyethyl)benzimidazoles have been prepared and the rate constants for their hydrolysis measured at various temperatures and oxonium ion concentrations.The formal kinetics followed and the effect of varying the 2-substitution on the hydrolysis rate suggest that the acid-catalyzed cleavage of these compounds involves a rapid initial protonation of the benzimidazole ring and a subsequent rate-limiting heterolysis of the protonated substrate to form a free nitrogen base and an oxocarbenium ion derived from the ethoxyethyl group.The values obtained for the entropy of activation are consistent with the assumed u nimolecular nature of the rate-limiting step.The effects of 2-substituents on the acidities of the protonated substrates and their heterolysis rates have been compared.The latter partial reaction has been suggested to be the subject of steric acceleration.

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