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132294-14-5

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132294-14-5 Usage

Physical state

Colorless liquid

Configuration

trans

Ethoxy group positioning

Opposite sides of the cyclobutane ring

Applications

Building block in the synthesis of pharmaceuticals and fine chemicals

Industry relevance

Pharmaceutical industry, specialty chemicals, and materials production

Safety concerns

Potential toxicity and flammability, requiring careful handling

Check Digit Verification of cas no

The CAS Registry Mumber 132294-14-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,2,9 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132294-14:
(8*1)+(7*3)+(6*2)+(5*2)+(4*9)+(3*4)+(2*1)+(1*4)=105
105 % 10 = 5
So 132294-14-5 is a valid CAS Registry Number.

132294-14-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (+/-)-trans-1,2-bis-(3,3-diethoxycyclobutylen)methanol

1.2 Other means of identification

Product number -
Other names trans-3,3-diethoxy-1,2-bis(hydroxymethyl)cyclobutane

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:132294-14-5 SDS

132294-14-5Relevant articles and documents

CYCLOBUTYL NUCLEOSIDE ANALOGS AS ANTI-VIRALS

-

Paragraph 0250; 0286, (2020/07/07)

Described herein are cyclobutyl nucleoside analogs of Formula (I), pharmaceutical compositions that include one or more cyclobutyl nucleoside analogs and methods of using the same to treat HBV, HDV and/or HIV.

Synthesis and antiviral activity of enantiomeric forms of cyclobutyl nucleoside analogues

Bisacchi,Braitman,Cianci,Clark,Field,Hagen,Hockstein,Malley,Mitt,Slusarchyk,Sundeen,Terry,Tuomari,Weaver,Young,Zahler

, p. 1415 - 1421 (2007/10/02)

The syntheses of the enantiomeric cyclobutyl guanine nucleoside analogues [1R-1α,2β,3α]- and [1S-1α,2β,3α]-2-amino-9-[2,3-bis(hydroxymethyl) cyclobutyl]-6H-purin-6-one (7 and 8, respectively) and the enantiomeric cyclobutyl adenine analogues [1R-1α,2β,3α]

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