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(5R,6S)-3-(Diphenoxy-phosphoryloxy)-6-[(R)-1-(4-nitro-benzyloxycarbonyloxy)-ethyl]-7-oxo-1-aza-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid 4-nitro-benzyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78072-36-3

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78072-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78072-36-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,0,7 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 78072-36:
(7*7)+(6*8)+(5*0)+(4*7)+(3*2)+(2*3)+(1*6)=143
143 % 10 = 3
So 78072-36-3 is a valid CAS Registry Number.

78072-36-3Relevant academic research and scientific papers

Studies on the Syntheses of Heterocyclic Compounds. Part 877. An Alternative Synthesis of Protected (+/-)-Thienamycin and a Related Compound

Kametani, Tetsuji,Huang, Shyh-Pyng,Nagahara, Takayasu,Yokohama, Shuichi,Ihara, Masataka

, p. 964 - 968 (2007/10/02)

An alternative total synthesis of protected (+/-)-thienamycin (2) and an analogue is described. (+/-)-4β-(2,2-Dimethoxyethyl)-3α-*)-1-(-nitrobenzyloxycarbonyloxy)ethyl>azetidin-2-one (5), prepared from isoxazoline derivatives (4), was conve

Total Synthesis of (+/-)-Epithienamycins A and B and Derivatives

Kametani, Tetsuji,Huang, Shyh-Pyng,Nagahara, Takayasu,Ihara, Masataka

, p. 2282 - 2286 (2007/10/02)

(+/-)-(3R*,4R*)-4-(2,2-Dimethoxyethyl)-3-*)-1-hydroxyethyl>azetidin-2-one (7), which has been stereoselectively synthesised via the 4-methoxycarbonylisoxazoline (4), was converted into (+/-)-epithienamycins A (2) and B

TOTAL SYNTHESIS OF (+/-)EPITHIENAMYCINS A AND B

Kametani, Tetsuji,Huang, Shyh-Pyng,Nagahara, Takayasu,Ihara, Masataka

, p. 65 - 70 (2007/10/02)

(+/-)-3R*-(1'S*-Hydroxyethyl)-4R*-(2',2'-dimethoxyethyl)-2-azetidinone (6), which was obtained from the 4-methoxycarbonylisoxazoline (4) as a major product, was converted into (+/-)-epithienamycins A(2) and B(3) vi

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