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4-[2-(4-methoxy-benzyloxy)ethyl]-2,2-dimethyl-[1,3]dioxolane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

167629-45-0

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167629-45-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 167629-45-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,6,2 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 167629-45:
(8*1)+(7*6)+(6*7)+(5*6)+(4*2)+(3*9)+(2*4)+(1*5)=170
170 % 10 = 0
So 167629-45-0 is a valid CAS Registry Number.

167629-45-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-(4-methoxy-benzyloxy)ethyl]-2,2-dimethyl-[1,3]dioxolane

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:167629-45-0 SDS

167629-45-0Relevant academic research and scientific papers

Isolation and synthesis of a novel β-carboline guanidine derivative tiruchanduramine from the Indian ascidian Synoicum macroglossum

Ravinder,Vijender Reddy,Krishnaiah,Ramesh,Ramakrishna,Laatsch,Venkateswarlu

, p. 5475 - 5478 (2007/10/03)

The isolation and synthesis of the racemic form of a novel β-carboline guanidine alkaloid, tiruchanduramine, a potent α-glucosidase inhibitor from the Indian ascidian, Synoicum macroglossum has been achieved.

A facile and convergent synthesis of sarmentosin

Xu, Rui,Bai, Donglu

, p. 3355 - 3363 (2007/10/03)

A concise synthesis of sarmentosin (1) starting from butane-1,2,4-triol-1,2-acetonide is described. This convergent route can also be employed for the preparation of sarmentosin analogues for structure-activity relationship studies.

Synthesis of aglycon analogues of sarmentosin and their bioactivity of lymphocyte proliferation.

Zhang, Hong,Xu, Rui,Hu, Zhongliang,He, Xuchang,Bai, Donglu,Li, Xiaoyu,Wang, Xiaofeng

, p. 3543 - 3545 (2007/10/03)

A number of aglycon analogues of sarmentosin were prepared and their bioactivities on the proliferation of T-lymphocytes and B-lymphocytes were assayed.

Synthesis of unsaturated carboacyclic nucleoside analogues via Mitsunobu reactions

Du, Jinfa,Wang, Guangyi

, p. 867 - 879 (2007/10/03)

2-Substituted allyl alcohols 9 and 14 were prepared starting from butane-1,2,4-triol and glycerol, respectively. Mitsunobu condensations of 9 and 14 with purine and pyrimidine bases, followed by deprotection, afforded a number of acyclonucleosides having

Terminal fluoroolefins. The synthesis of novel carboacyclic nucleosides

Miller, Shawn C.,McCarthy, James R.,Sabol, Jeffrey S.

, p. 1099 - 1113 (2007/10/03)

A facile preparation of ketone 7 from butanetriol acetonide 5 is reported, and its utility for the synthesis of novel carboacyclic nucleosides 3E, 3Z, 4E and 4Z by the selective manipulation of multiple functionalities is demonstrated.

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