추천 제품
분석
96%
형태
liquid
광학 활성
[α]20/D −8.5°, c = 1.5 in acetone
광학 순도
ee: ≥96.0% (GLC)
refractive index
n20/D 1.425 (lit.)
bp
84-86 °C/15 mmHg (lit.)
density
1.106 g/mL at 25 °C (lit.)
SMILES string
COC(=O)[C@@H]1COC(C)(C)O1
InChI
1S/C7H12O4/c1-7(2)10-4-5(11-7)6(8)9-3/h5H,4H2,1-3H3/t5-/m0/s1
InChI key
DOWWCCDWPKGNGX-YFKPBYRVSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
(−)-Methyl (S)-2,2-dimethyl-1,3-dioxolane-4-carboxylate can be used:
- As a chiral building block to make the key tetrahydrofuran subunit of (−)-gymnodimine, a marine algal toxin.
- To prepare an enedione by reacting with dimethyl methylphosphonate, BuLi, and phenylglyoxal, which in turn is used to synthesize cyclopentenone derivatives.
- As a starting material for the preparation of (S)-4,5-dihydroxy-2,3-pentanedione (DPD), a precursor for autoinducer (AI)-2 in bacteria.
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
172.4 °F - closed cup
Flash Point (°C)
78 °C - closed cup
개인 보호 장비
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
Annulation of 2-Oxoalkylidenetriphenylphosphoranes with enediones: A one-step synthesis of substituted cyclopentenones
Synthesis, 2002(06), 0739-0744 (2002)
The Journal of biological chemistry, 280(20), 19563-19568 (2005-03-26)
We describe an original, short, and convenient chemical synthesis of enantiopure (S)-4,5-dihydroxy-2,3-pentanedione (DPD), starting from commercial methyl (S)-(-)-2,2-dimethyl-1,3-dioxolane-4-carboxylate. DPD is the precursor of autoinducer (AI)-2, the proposed signal for bacterial interspecies communication. AI-2 is synthesized by many bacterial species in
Studies on the Synthesis of (−)-Gymnodimine. Subunit Synthesis and Coupling
The Journal of Organic Chemistry, 72(5), 1717-1728 (2007)
The Journal of organic chemistry, 72(5), 1717-1728 (2007-02-01)
Two principal subunits of the marine algal toxin (-)-gymnodimine were synthesized. A trisubstituted tetrahydrofuran representing C10-C18 of the toxin was prepared via a highly stereoselective iodine-mediated cyclization of an acyclic alkene bearing a bis-2,6-dichlorobenzyl (DCB) ether. The formation of a
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