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122087-86-9

122087-86-9

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122087-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122087-86-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,0,8 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 122087-86:
(8*1)+(7*2)+(6*2)+(5*0)+(4*8)+(3*7)+(2*8)+(1*6)=109
109 % 10 = 9
So 122087-86-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO2/c1-5(11)10-7-4-6-2-3-8(12)9(6)7/h2-4,6,9H,1H3,(H,10,11)

122087-86-9SDS

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-(4-oxo-6-bicyclo[3.2.0]hepta-2,6-dienyl)acetamide

1.2 Other means of identification

Product number -
Other names 7-Aabhdo

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:122087-86-9 SDS

122087-86-9Downstream Products

122087-86-9Relevant articles and documents

CHIRAL LASER PHOTOCHEMISTRY : PHOTORESOLUTION ACCOMPANYING PHOTOISOMERIZATION OF (+/-)-1-ACETYL(BENZOYL)AMINOBICYCLOHEPTA-3,6-DIEN-2-ONE TO OPTICALLY ACTIVE 7-ISOMERS. A PHOTOCHEMICAL PROCDURE FOR CHIRALITY ENHANCEMENT OF (-)-(1S,5S)-7-ACETYLAMINOBICYCLOHEPTA-3,6-DIEN-2-ONE

Cavazza, Marino,Morganti, Gioia,Zandomeneghi, Maurizio

, p. 891 - 896 (2007/10/02)

Photoisomerization of (+/-)-1-acetylaminobicyclohepta-3,6-dien-2-one (+/-)-2b with u.v. left circularly polarized light up to 36percent conversion led to (-)-(1S,5R)-(2b) max. (347)-4.2 dm3 mol-1 cm-1> and (-)-(1S,5S)-7-acetylaminobicyclohepta-3,6-dien-2-one (-)-(3b) max. (345) -3.3>.The optical purities obtained allowed us to measure circular dichroism for λ > 260 nm.An analogous procedure when applied to the benzoylamino-derivatives gave Δεmax. (348) -5.0 and Δεmax. (346) -4.9 for the 1- and 7- derivatives, respectively.Further chirality enhancement to o.p. 2.9percent permitted a complete (>200 nm) c.d. spectrum to be obtained for (-)-(3b).

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