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79320-86-8

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  • Spiro[4,10-methano[1]benzoxepino[3,4-d]oxazole-11, 2-oxirane]-9a(5aH)-methanol, 3a,4,8,9,10, 10a-hexahydro-3a-hydroxy-2,7,10-trimethyl-, .alpha.-acetate, (3a.alpha.,4.beta.,5a.alpha.,9a.alpha.,10.beta

    Cas No: 79320-86-8

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  • Spiro[4,10-methano[1]benzoxepino[3,4-d]oxazole-11, 2-oxirane]-9a(5aH)-methanol, 3a,4,8,9,10, 10a-hexahydro-3a-hydroxy-2,7,10-trimethyl-, .alpha.-acetate, (3a.alpha.,4.beta.,5a.alpha.,9a.alpha.,10.beta

    Cas No: 79320-86-8

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79320-86-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79320-86-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,2 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79320-86:
(7*7)+(6*9)+(5*3)+(4*2)+(3*0)+(2*8)+(1*6)=148
148 % 10 = 8
So 79320-86-8 is a valid CAS Registry Number.

79320-86-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Spiro[4,10-methano[1]benzoxepino[3,4-d]oxazole-11,2'-oxirane]-9a(5aH)-methanol, 3a,4,8,9,10,10a-hexahydro-3a-hydroxy-2,7,10-trimethyl-, .α.-acetate, (3a.α.,4.β.,5a.α.,9a.α.,10.β.,10a.α.,11S*)-

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

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More Details:79320-86-8 SDS

79320-86-8Upstream product

79320-86-8Downstream Products

79320-86-8Relevant articles and documents

Reductive amination of 3-Ketoanguidin and Antitumor Activity of the Products

Kaneko, T.,Wong, H.,Howell, H. G.,Rose, W. C.,Bradner, W. T.,Doyle, T. W.

, p. 958 - 960 (2007/10/02)

Amine-containing trichothecanes were prepared by reductive aminations of 3-ketoanguidin.In in vivo tests against P388 leukemia, most of them showed an improved activity compared to anguidin though their potency was decreased. 3-Ketoanguidin also produced some unexpected structures: oxazoline 5, dioxaline 7, and α-amino nitrile 13.

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