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[5-(4-chloro-phenyl)-5-oxo-pentyl]-carbamic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

215720-35-7

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215720-35-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 215720-35-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,7,2 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 215720-35:
(8*2)+(7*1)+(6*5)+(5*7)+(4*2)+(3*0)+(2*3)+(1*5)=107
107 % 10 = 7
So 215720-35-7 is a valid CAS Registry Number.

215720-35-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-[5-(4-chlorophenyl)-5-oxopentyl]carbamate

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:215720-35-7 SDS

215720-35-7Relevant academic research and scientific papers

DNA-damaging steroidal alkaloids from Eclipta alba from the suriname rainforest

Abdel-Kader, Maged S.,Bahler, Brian D.,Malone, Stan,Werkhoven, Marga C. M.,Van Troon, Frits,David,Wisse, Jan H.,Bursuker, Isia,Neddermann, Kim M.,Mamber, Stephen W.,Kingston, David G. I.

, p. 1202 - 1208 (2007/10/03)

Bioassay-guided fractionation of the MeOH extract of Eclipta alba using three yeast strains (1138, 1140, and 1353) resulted in the isolation of eight bioactive steroidal alkaloids (1-8), six of which are reported for the first time from nature. The major alkaloid was identified as (20S)(25S)-22,26- imino-cholesta-5,22(N)-dien-3β-ol (verazine, 3), while the new alkaloids were identified as 20-epi-3-dehydroxy-3-oxo-5,6-dihydro-4,5-dehydroyerazine (1), ecliptalbine [(20R)-20-pyridyl-cholesta-5-ene-3β,23-diol] (4), (20R)- 4β-hydroxyverazine (5), 4β-hydroxyverazine (6), (20R)-25β-hydroxyverazine (7), and 25β-hydroxyverazine (8). Ecliptalbine (4), in which the 22,26- imino ring of verazine was replaced by a 3-hydroxypyridine moiety, had comparable bioactivity to verazine in these assays, while a second alkaloid (8) showed good activity against Candida albicans. All the alkaloids showed weak cytotoxicity against the M-109 cell line.

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