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75488-69-6

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75488-69-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75488-69-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,4,8 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75488-69:
(7*7)+(6*5)+(5*4)+(4*8)+(3*8)+(2*6)+(1*9)=176
176 % 10 = 6
So 75488-69-6 is a valid CAS Registry Number.

75488-69-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(9-ethoxy-1,2,3-trimethoxy-10-oxo-6,7-dihydro-5H-benzo[a]heptalen-7-yl)acetamide

1.2 Other means of identification

Product number -
Other names N-((S)-9-Aethoxy-1,2,3-trimethoxy-10-oxo-5,6,7,10-tetrahydro-benzo[a]heptalen-7-yl)-acetamid

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:75488-69-6 SDS

75488-69-6Downstream Products

75488-69-6Relevant articles and documents

Synthesis of 1,3-diazaazulene derivatives of colchicinoids and isocolchicinoids via ipso- or tele-substitution-condensation with amidines

Cavazza, Marino,Pietra, Francesco

, p. 14059 - 14064 (1998)

Condensation of colchicinoids and isocolchicinoids with amidines in dry benzene affords regioselectively 1,3-diazaazulene derivatives: ipso- substitution-condensation products (e.g. 7) are best obtained from cycloheptatrienone-ring deactivated substrates (e.g. 4), whereas isomeric tele-substitution-condensation products (e.g. 13), are best accessible from cycloheptatrienone-ring activated substrates (e.g. 10). Hydroxylic solvents inhibit tele-substitution-condensation, arguably by undergoing protonation in preference of the intermediate σ adduct.

Comparison of inhibitory effects of colchicine, isocolchicine and homologous compounds on cell division.

LETTRE,FERNHOLZ

, p. 123 - 127 (2007/10/12)

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