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110652-72-7

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110652-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110652-72-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,6,5 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 110652-72:
(8*1)+(7*1)+(6*0)+(5*6)+(4*5)+(3*2)+(2*7)+(1*2)=87
87 % 10 = 7
So 110652-72-7 is a valid CAS Registry Number.
InChI:InChI=1/C19H23N3O4/c1-21(2)16(23)9-8-12-10-14-18(26-4)20-17-13(19(24)22(14)11-12)6-5-7-15(17)25-3/h5-9,11,14,18,20H,10H2,1-4H3/b9-8+/t14?,18-/m1/s1

110652-72-7SDS

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 (E)-3-[(6R)-4,6-dimethoxy-11-oxo-5,6,6a,7-tetrahydropyrrolo[2,1-c][1,4]benzodiazepin-8-yl]-N,N-dimethylprop-2-enamide

1.2 Other means of identification

Product number -
Other names Porothramycin B

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:110652-72-7 SDS

110652-72-7Downstream Products

110652-72-7Related news

Enantioselective synthesis of (+) porothramycin B (cas 110652-72-7) and its 9-Demethoxy analogue08/16/2019

(+) 9-Demethoxyporothramycin B 3a and (+) porothramycin B 3b were synthesized from (S) pyroglutamic acid through a versatile and efficient route.detailed

110652-72-7Relevant articles and documents

Total synthesis of (+)-porothramycin B

Fukuyama, Tohru,Liu, Gang,Linton, Steven D.,Lin, Shao-Cheng,Nishino, Hiroshi

, p. 2577 - 2580 (2007/10/02)

The first total synthesis of (+)-porothramycin B (1b is described. Our synthetic pathway can be readily applied to the synthesis of other members of the pyrrolo[1,4]benzodiazepine antibiotics.

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