130369-33-4

Basic information

• Product Name: (3,3-dimethoxycyclobutane-1,1-diyl)dimethanol
• Synonyms: (3,3-dimethoxycyclobutane-1,1-diyl)dimethanol
• CAS NO: 130369-33-4
• Molecular Weight: 176.213
• Mol File: 130369-33-4.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: (3,3-dimethoxycyclobutane-1,1-diyl)dimethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (3,3-dimethoxycyclobutane-1,1-diyl)dimethanol(130369-33-4)
• EPA Substance Registry System: (3,3-dimethoxycyclobutane-1,1-diyl)dimethanol(130369-33-4)

Safety Data

• Hazardous Substances Data: 130369-33-4(Hazardous Substances Data)

Usage

General Description

(3,3-dimethoxycyclobutane-1,1-diyl)dimethanol is a chemical compound with the molecular formula C8H16O4. It is a cyclic diol compound that contains two methoxy groups and a cyclobutane ring. (3,3-dimethoxycyclobutane-1,1-diyl)dimethanol is commonly used in organic synthesis and as a building block in the formation of more complex organic molecules. It has potential applications in the pharmaceutical, agrochemical, and materials science industries due to its unique structural properties and reactivity. Additionally, it can serve as a valuable intermediate in the synthesis of various organic compounds, making it a versatile and important chemical in the field of organic chemistry.

Upstream product

• 115118-67-7 diethyl 3,3-dimethoxycyclobutane-1,1-dicarboxylate 
• 115118-68-8 3,3-dimethoxycyclobutane-1,1-dicarboxylic acid diisopropyl ester 

Downstream Products

• 1023815-74-8 (3,3-dimethoxycyclobutane-1,1-diyl)bis(methylene) bis(4-methylbenzenesulfonate) 
• 130368-81-9 9-<3,3-bis(hydroxymethyl)cyclobut-1-yl>guanine 
• 131853-47-9 9-<3,3-bis(hydroxymethyl)cyclobut-1-yl>adenine 
• 131853-56-0 9-<3,3-bis(benzyloxymethyl)cyclobut-1-yl>guanine 
• 131853-55-9 2-amino-6-chloro-9-<3,3-bis(benzyloxymethyl)cyclobut-1-yl>-9H-purine 
• 131853-53-7 2,5-diamino-6-chloro-4-<<3,3-bis(benzyloxymethyl)cyclobut-1-yl>amino>pyrimidine 
• 131853-57-1 9-<3,3-bis(benzyloxymethyl)cyclobut-1-yl>adenine 
• 131853-54-8 6-chloro-9-<3,3-bis(benzyloxymethyl)cyclobut-1-yl>-9H-purine 
• 131853-52-6 5-amino-6-chloro-4-<<3,3-bis(benzyloxymethyl)cyclobut-1-yl>amino>pyrimidine 
• 131853-58-2 9-<3-benzyloxymethyl-3-hydroxymethylcyclobut-1-yl>adenine 
• 131853-51-5 3,3-bis(benzyloxymethyl)cyclobutanone oxime 
• 131853-50-4 3,3-bis(benzyloxymethyl)cyclobutanone 
• 131853-48-0 1-amino-3,3-bis(benzyloxymethyl)cyclobutane 
• 305819-04-9 C₄₂H₄₄O₉S₂ 

Relevant articles and documents

NOVEL DUAL MODE OF ACTION SOLUBLE GUANYLATE CYCLASE ACTIVATORS AND PHOSPHODIESTERASE INHIBITORS AND USES THEREOF

The present invention relates to compounds of formula (I), or pharmaceutically acceptable salt, solvate or hydrate thereof, wherein said compound of formula (I) comprises at least one covalently bound -ONO2 or -ONO moiety and at most four covalently bound -ONO2 or -ONO moieties, and wherein AR, R1, X, R3 and R4 are as defined in claim 1; and pharmaceutical compositions thereof, and their use in methods of treating or preventing a disease alleviated by inhibition of PDE5 in a human or in a non-human mammal.

Synthesis of 2-azaspiro[3.3]heptane-derived amino acids: Ornitine and GABA analogues

Synthesis of 6-amino-2-azaspiro[3.3]heptane-6-carboxylic acid and 2-azaspiro[3.3]heptane-6-carboxylic acid was performed. Both four-membered rings in the spirocyclic scaffold were constructed by subsequent ring closure of corresponding 1,3-bis-electrophil

Synthesis of conformationally restricted glutamic acid analogs based on the spiro[3.3]heptane scaffold

A library of isomeric glutamic acid analogs based on the spiro[3.3]heptane skeleton is designed. Two members of the library, (R)- and (S)-2-amino-spiro[3.3]heptane-2,6-dicarboxylic acid hydrochlorides, were synthesized. The stereochemistry of the synthesi