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92935-94-9

"Angelicide" is a term that does not refer to a specific chemical compound but rather seems to be a fictional or metaphorical term. It does not appear in standard chemical databases or scientific literature. The term might be used in a creative or artistic context to evoke a sense of something that destroys or neutralizes the qualities associated with angels. Without a specific chemical definition or context, it's not possible to provide a summary of "Angelicide" as a chemical. If you are referring to a different chemical or have a specific context in mind, please provide additional details so I can assist you further.

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  • 92935-94-9 Structure

  • Basic information

    1. Product Name: Angelicide
    2. Synonyms: Angelicide;3-Butylidene-3,4,5,5a,6,6',7',7a-octahydro-6-propylspiro[cyclobut[e]isobenzofuran-7(1H),1'(3'H)-isobenzofuran]-1,3'-dione
    3. CAS NO:92935-94-9
    4. Molecular Formula: C24H28O4
    5. Molecular Weight: 380.48
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92935-94-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Angelicide(CAS DataBase Reference)
    10. NIST Chemistry Reference: Angelicide(92935-94-9)
    11. EPA Substance Registry System: Angelicide(92935-94-9)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 92935-94-9(Hazardous Substances Data)

92935-94-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92935-94-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,3 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92935-94:
(7*9)+(6*2)+(5*9)+(4*3)+(3*5)+(2*9)+(1*4)=169
169 % 10 = 9
So 92935-94-9 is a valid CAS Registry Number.

92935-94-9SDS

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 riligustilide

1.2 Other means of identification

Product number -
Other names -

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:92935-94-9 SDS

92935-94-9Upstream product

92935-94-9Downstream Products

92935-94-9Relevant articles and documents

Triangeliphthalides A-D: Bioactive phthalide trimers with new skeletons from: Angelica sinensis and their production mechanism

Zou, Jian,Chen, Guo-Dong,Zhao, Huan,Wang, Xiao-Xia,Zhang, Zai-Jun,Qu, Yi-Bo,He, Rong-Rong,So, Kwok-Fai,Yao, Xin-Sheng,Gao, Hao

supporting information, p. 6221 - 6224 (2019/06/07)

Triangeliphthalides A-D (1-4), four novel phthalide trimers with two new linkage styles, were isolated from Angelica sinensis, together with two related phthalide dimers (5-6). Their structures including absolute configurations were determined. The production mechanism of phthalide polymers was proposed, and their bioactivities were also evaluated.

Triligustilides A and B: Two Pairs of Phthalide Trimers from Angelica sinensis with a Complex Polycyclic Skeleton and Their Activities

Zou, Jian,Chen, Guo-Dong,Zhao, Huan,Huang, Ying,Luo, Xiang,Xu, Wei,He, Rong-Rong,Hu, Dan,Yao, Xin-Sheng,Gao, Hao

supporting information, p. 884 - 887 (2018/02/10)

Two pairs of enantiomeric phthalide trimers [(-)/(+) triligustilides A (1a/1b) and (-)/(+) triligustilides B (2a/2b)] with complex polycyclic skeletons simultaneously possessing bridged, fused, and spiro ring systems were isolated from Angelica sinensis, together with two pairs of new phthalide dimers. The biogenetic pathways of new phthalides were proposed, and their bioactivities were also evaluated. This is the first time optically pure polymeric phthalides have been obtained from racemates, and their absolute configurations are reported.

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