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1674-01-7

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1674-01-7 Usage

General Description

(7R)-5-Ethyl-1,4,7,8,9,10-hexahydro-2H-3,7-methanoazacycloundecino[5,4-b]indole is a chemical compound with a complex molecular structure. It contains a hexahydro-fused indole ring system with a ethyl group attached at the 5-position. (7R)-5-Ethyl-1,4,7,8,9,10-hexahydro-2H-3,7-methanoazacycloundecino[5,4-b]indole has potential pharmaceutical applications as it may exhibit biological activity due to its unique structure and functional groups. Its specific properties and uses would need to be determined through further research and testing.

Check Digit Verification of cas no

The CAS Registry Mumber 1674-01-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,7 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1674-01:
(6*1)+(5*6)+(4*7)+(3*4)+(2*0)+(1*1)=77
77 % 10 = 7
So 1674-01-7 is a valid CAS Registry Number.

1674-01-7SDS

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 (+)-cleavamine

1.2 Other means of identification

Product number -
Other names Cleavamin

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:1674-01-7 SDS

1674-01-7Downstream Products

1674-01-7Relevant articles and documents

CHIRALITY CONTROL BY KINETIC PROTONATION: ENANTIOSELECTIVE SYNTHESES OF (+)-VELBANAMINE, (-)-ISOVELBANAMINE, AND (+)-CLEAVAMINE

Takano, Seiichi,Uchida, Wataru,Hatakeyama, Susumi,Ogasawara, Kunio

, p. 733 - 736 (2007/10/02)

Optimal conditions for inversion of chirality at 2-position of the 2-alkyllactone(5) have been established.By utilizing the inversion method developed, three indole alkaloids, (+)-velbanamine(16), (-)-isovelbanamine(17), and (+)-cleavamine(18), have been synthesized from the chiral lactone(1) which has been previously used for the syntheses of the enantiomers of these alkaloids.

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