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91511-88-5

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91511-88-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91511-88-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,5,1 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91511-88:
(7*9)+(6*1)+(5*5)+(4*1)+(3*1)+(2*8)+(1*8)=125
125 % 10 = 5
So 91511-88-5 is a valid CAS Registry Number.

91511-88-5Relevant articles and documents

Synthesis of phenylbutadiynylpyridinium derivatives for nonlinear optics

Kan-No, Shin-Ya,Okada, Shuji

, p. 365 - 371 (2007)

1-Methyl-4-{[4-(dimethylamino)phenyl]butadiynyl}pyridinium (PBP) derivatives with iodide or benzenesulfonate anion were synthesized as potential compounds for both second- and third-order NLO applications. PBP shows peculiar absorption spectrum in methano

Tuning of cross-Glaser products mediated by substrate-catalyst polymeric backbone interactions

Ali, Md. Ehesan,Dar, Arif Hassan,Gowri, Vijayendran,Jayamurugan, Govindasamy,Kaur, Sharanjeet,Mukhopadhyaya, Aritra,Neethu, K. M.,Sartaliya, Shaifali,Selim, Abdul

supporting information, p. 2582 - 2585 (2020/03/10)

Tuning of cross-Glaser products using different polymeric backbones supported by copper oxide nano-catalysts has been demonstrated by tweaking the substrate-catalyst interactions under greener conditions. Further, highly reactive magnetically separable and recyclable catalyst with scalability is demonstrated.

Trisulfur radical anion as the key intermediate for the synthesis of thiophene via the interaction between elemental sulfur and NaO t Bu

Zhang, Guoting,Yi, Hong,Chen, Hong,Bian, Changliang,Liu, Chao,Lei, Aiwen

supporting information, p. 6156 - 6159 (2015/01/16)

A facile base-promoted sulfur-centered radical generation mode and a single-step protocol for the synthesis of thiophene derivatives using 1,3-diynes via the interaction between elemental sulfur and NaOtBu has been reported. EPR experiments revealed that the trisulfur radical anion acts as a key intermediate of this process. A plausible mechanism has been proposed.

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