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78774-88-6

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78774-88-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78774-88-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,7,7 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 78774-88:
(7*7)+(6*8)+(5*7)+(4*7)+(3*4)+(2*8)+(1*8)=196
196 % 10 = 6
So 78774-88-6 is a valid CAS Registry Number.

78774-88-6SDS

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 1-[(2-bromophenyl)methyl]-1,2,3,4-tetrahydroisoquinoline

1.2 Other means of identification

Product number -
Other names 1-(2-bromobenzyl)-1,2,3,4-tetrahydroisoquinoline

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:78774-88-6 SDS

78774-88-6Relevant articles and documents

Alkaloid constituents from flower buds and leaves of sacred lotus (Nelumbo nucifera, Nymphaeaceae) with melanogenesis inhibitory activity in B16 melanoma cells

Nakamura, Seikou,Nakashima, Souichi,Tanabe, Genzo,Oda, Yoshimi,Yokota, Nami,Fujimoto, Katsuyoshi,Matsumoto, Takahiro,Sakuma, Rika,Ohta, Tomoe,Ogawa, Keiko,Nishida, Shino,Miki, Hisako,Matsuda, Hisashi,Muraoka, Osamu,Yoshikawa, Masayuki

, p. 779 - 787 (2013/02/25)

Methanolic extracts from the flower buds and leaves of sacred lotus (Nelumbo nucifera, Nymphaeaceae) were found to show inhibitory effects on melanogenesis in theophylline-stimulated murine B16 melanoma 4A5 cells. From the methanolic extracts, a new alkaloid, N-methylasimilobine N-oxide, was isolated together with eleven benzylisoquinoline alkaloids. The absolute stereostructure of the new alkaloid was determined from chemical and physicochemical evidence. Among the constituents isolated, nuciferine, N-methylasimilobine, (-)-lirinidine, and 2-hydroxy-1-methoxy-6a,7-dehydroaporphine showed potent inhibition of melanogenesis. Comparison of the inhibitory activities of synthetic related alkaloids facilitated characterization of the structure-activity relationships of aporphine- and benzylisoquinoline-type alkaloids. In addition, 3-30 μM nuciferine and N-methylasimilobine inhibited the expression of tyrosinase mRNA, 3-30 μM N-methylasimilobine inhibited the expression of TRP-1 mRNA, and 10-30 μM nuciferine inhibited the expression of TRP-2 mRNA.

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