Cas 1166-94-5,4aα,7-Dihydroxy-1β,8-dimethyl-gibb-2-en-1α,10β-dicarbonsaeure-10-methylester-1.4a-lacton

1166-94-5

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Basic information

Product Name: 4aα,7-Dihydroxy-1β,8-dimethyl-gibb-2-en-1α,10β-dicarbonsaeure-10-methylester-1.4a-lacton
Synonyms:
CAS NO:1166-94-5
Molecular Formula:
Molecular Weight: 346.423
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4aα,7-Dihydroxy-1β,8-dimethyl-gibb-2-en-1α,10β-dicarbonsaeure-10-methylester-1.4a-lacton(CAS DataBase Reference)
NIST Chemistry Reference: 4aα,7-Dihydroxy-1β,8-dimethyl-gibb-2-en-1α,10β-dicarbonsaeure-10-methylester-1.4a-lacton(1166-94-5)
EPA Substance Registry System: 4aα,7-Dihydroxy-1β,8-dimethyl-gibb-2-en-1α,10β-dicarbonsaeure-10-methylester-1.4a-lacton(1166-94-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1166-94-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1166-94-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,6 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1166-94:
(6*1)+(5*1)+(4*6)+(3*6)+(2*9)+(1*4)=75
75 % 10 = 5
So 1166-94-5 is a valid CAS Registry Number.

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1166-94-5Downstream Products

1166-94-5Relevant academic research and scientific papers

Inhibitors of the Biosynthesis of Gibberellins. Part 1. 7-Fluoro-10β-fluoromethyl-1β,8-dimethylgibbane-1α,4aα-carbolactone

Boulton, Keith,Cross, Brian E.

, p. 427 - 432 (2007/10/02)

The title compound (1) has been prepared from gibberellic acid; its addition to a fermentation of G. fujikuroi led to the accumulation of ent-kaurene, and hence suggested that it inhibited the biosynthetic oxidation of kaurene.Compound (1) also retards the conversion of gibberellin A12 aldehyde (25) into gibberellins A12 (26) and A43 (21) by a plant enzyme system.

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