4-chloromethyl-5-methyl-1,3-Dioxol-2-one

Intermediate API Family: Olmesartan CAT No. CS-O-31596 CAS No. 80841-78-7
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Product Detail

4-chloromethyl-5-methyl-1,3-Dioxol-2-one

Olmesartan Intermediate
Stock Status: In Stock  Login to view price
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For Research & Analytical Purposes. Not for Personal use.
Category Intermediate
API Family Olmesartan
Storage Store at refrigerator (2-8°C) for long term storage
Hazard Information Refer MSDS for accurate information.

4-chloromethyl-5-methyl-1,3-Dioxol-2-one Product Information

4-chloromethyl-5-methyl-1,3-Dioxol-2-one is listed under Intermediate. It is associated with Olmesartan and is intended for analytical research, quality control and pharmaceutical reference standard applications. The product is supplied by Clearsynth under CAT No. CS-O-31596.

Clearsynth provides this compound for research and analytical use, with product information including CAS number, molecular formula, molecular weight, stock enquiry details and supporting documentation.

Technical Data

Product Name
4-chloromethyl-5-methyl-1,3-Dioxol-2-one
CAS No.
80841-78-7
CAT No.
CS-O-31596
Molecular Formula
C5H5ClO3
Molecular Weight
148.5
Category
API Family
Storage Condition
Store at refrigerator (2-8°C) for long term storage
SMILES
O=C1OC(CCl)=C(C)O1
IUPAC Name
"(5-Methyl-2-oxo-1,3-dioxol-4-yl)methyl Chloride; 4-Chloromethyl-5-methyl-2-oxo-1,3-dioxole;"
Purity by HPLC
>98%
Hazard Compound
Refer MSDS for accurate information.

Description

Overview
"4-Chloromethyl-5-methyl-1,3-dioxol-2-one is an important reagent in the preparation of angiotensin II receptor antagonist such as Olmesratan Medoxomil (O550000). 4-Chloromethyl-5-methyl-1,3-dioxol-2-one is also used in the preparation of prodrugs of ampicillin."
Synonyms
"(4-(Chloromethyl)-5-methyl-1,3-Dioxol-2-one)"
Application Notes
"4-Chloromethyl-5-methyl-1,3-dioxol-2-one is an important reagent in the preparation of angiotensin II receptor antagonist such as Olmesratan Medoxomil (O550000). 4-Chloromethyl-5-methyl-1,3-dioxol-2-one is also used in the preparation of prodrugs of ampicillin."
References
"Ikeda, S, et al,: Chem, Pharmac, Bull,, 32, 4316 (1984); Wu, T, Yaox, Xueb,, 41, 537 (2006);"
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