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70905-45-2

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70905-45-2 Usage

Uses

1,3-Dichloro-2-(methoxymethoxy)propane (cas# 70905-45-2) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 70905-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,9,0 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 70905-45:
(7*7)+(6*0)+(5*9)+(4*0)+(3*5)+(2*4)+(1*5)=122
122 % 10 = 2
So 70905-45-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H10Cl2O2/c1-8-4-9-5(2-6)3-7/h5H,2-4H2,1H3

70905-45-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dichloro-2-(methoxymethoxy)propane

1.2 Other means of identification

Product number -
Other names 1,1-Bis(chloromethyl)-2,4-dioxapentane

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:70905-45-2 SDS

70905-45-2Relevant articles and documents

Novel nucleoside analogues as effective antiviral agents for Zika virus infections

Bassetto, Marcella,Basso, Mattia,Brancale, Andrea,Bugert, Joachim J.,Cima, Cecilia M.,Friese, Daniela,Salerno, Martina,Schwarze, Frank

, (2020/10/29)

Previously considered a neglected flavivirus, Zika virus has recently emerged as a public health concern due to its ability to spread rapidly and cause severe neurological disorders, such as microcephaly in newborn babies from infected mothers, and Guilla

A unified approach to the enantioselective synthesis of 2,6-cis and trans disubstituted tetrahydropyranones

Crimmins, Michael T.,Diaz, Caroline J.,Emmitte, Kyle A.

, p. 179 - 183 (2007/10/03)

A stereoselective construction of cis- and trans-2,6-disubstituted tetrahydropyranones, based on strategy which combines an asymmetric alkylation and ring closing metathesis for the formation of a cyclic enol ether, is reported.

An efficient synthesis of 2-[(4-amino-1,2-dihydro-2-oxo-1- pyrimidinyl)methoxy]-1,3-propanediyl-di-L-valinate an anti-cytomegalovirus agent

Ghali,Johnston,Beauchamp,Naseree,Scott,Flanagan,Rodriguez

, p. 1591 - 1600 (2007/10/02)

An efficient synthesis for large scale preparation of the titled compound, a prodrug for the anti-HCMV agent 1-[2-hydroxy-1- (hydroxymethyl)ethoxy)methyl]cytosine, 9, has been developed. The product of each step is easily purified by either distillation o

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