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(3S,3aS,6aR,7aR,8aS,8bS,8cS)-3,8a-dimethyl-6-methylidenedecahydrooxireno[2,3]azuleno[4,5-b]furan-2(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75956-97-7

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75956-97-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75956-97-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,9,5 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 75956-97:
(7*7)+(6*5)+(5*9)+(4*5)+(3*6)+(2*9)+(1*7)=187
187 % 10 = 7
So 75956-97-7 is a valid CAS Registry Number.

75956-97-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (11S)-3β,4β-epoxy-10(14)eno-12,6α-lactone

1.2 Other means of identification

Product number -
Other names (3S,3aS,6aR,7aS,8bS,8cS)-3,8a-Dimethyl-6-methylene-decahydro-1,8-dioxa-cyclopenta[h]cyclopropa[a]azulen-2-one

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:75956-97-7 SDS

75956-97-7Upstream product

75956-97-7Relevant academic research and scientific papers

Studies on the Syntheses of Sesquiterpene Lactones. 11. The Syntheses of 3-Epizaluzanin C, Zaluzanin C, Zaluzanin D, and Related Compounds 3&α-Hydroxyguaia-1(10),4(15),11(13)-trieno-12,6&α-lactone and 3&α-Hydroxyguaia-4(15),9,11(13)-trieno-12,6&α-lactone

Ando, Masayoshi,Kusaka, Haruhiko,Ohara, Hiroshi,Takase, Kahei,Yamaoka, Hiroaki,Yanagi, Yoshikazu

, p. 1952 - 1960 (2007/10/02)

3-Epizaluzanin C (10), 3α-hydroxyguaia-1(10),4(15),11(13)-trieno-12,6α-lactone (36), and 3α-hydroxyguaia-4(15),9,11(13)-trieno-12,6α-lactone (37) have been synthesized in 4.0percent, 3.0percent, and 1.7percent overall yields, respectively, from α-santonine (13) in 14 steps.Zaluzanin C (11) and zaluzanin D (12) have also been synthesized in 2.4percent and 2.5percent overall yields from α-santonin (13) in 16 steps and 15 steps, respectively.The key step involves the solvolytic rearrangement of (11S)-3α,4α-epoxy-1β-(mesyloxy)eudesmano-13,6α-lactone (27).The stereochemistry of3-epizaluzanin C (10), zaluzanin C (11), and zaluzanin D (12) have been established by these stereospecific syntheses.

TOTAL SYNTHESIS OF ZALUZANIN C, ZALUZANIN D, AND 3-EPIZALUZANIN C

Ando, Masayoshi,Yamaoka, Hiroaki,Takase, Kahei

, p. 501 - 504 (2007/10/02)

The biologically active guaianolides, zaluzanin C, and zaluzanin D, and the stereoisomeric guaianolide, 3-epizaluzanin C have been synthesized by two different procedures.The stereochemistry at C3 of zaluzanin C has been established to be S configuration by this synthesis.

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